Canonical Allele Identifier: CA916084431

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806566_47806567insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA , CM000664.2:g.47806566_47806567insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA GRCh38
NC_000002.11:g.48033705_48033706insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA , CM000664.1:g.48033705_48033706insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA GRCh37
NC_000002.10:g.47887209_47887210insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA NCBI36
NG_007111.1:g.28420_28421insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA , LRG_219:g.28420_28421insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA
NG_008397.1:g.104109_104110insTCTCAAATTCTCTTGCTTTTCTATGTCCCTTTTGAATAACTTCCTCTGGGAGATTAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000406248.2:p.Ala1207GlyfsTer2
ENST00000420813.6:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000390382.2:p.Ala1207GlyfsTer2
ENST00000455383.6:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000397484.2:p.Ala1207GlyfsTer2
ENST00000700004.2:c.3532_3533insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000514752.2:p.Ala1178GlyfsTer2
ENST00000699999.1:n.4590_4591insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700000.1:c.2350_2351insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000514749.1:p.Ala784GlyfsTer2
ENST00000700002.1:c.3922_3923insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000514750.1:p.Ala1308GlyfsTer2
ENST00000700003.1:c.1371_1372insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000514751.1:n.1371_1372insGCTAATCTCCCAGAGGAAGTTATTCAAAA...
ENST00000700004.1:c.2689_2690insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000514752.1:p.Ala897GlyfsTer2
ENST00000700005.1:n.2767_2768insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700006.1:n.5074_5075insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700007.1:n.2511_2512insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700008.1:n.2178_2179insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700009.1:n.2580_2581insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700010.1:n.1325_1326insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000700011.1:n.3210_3211insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6)
ENST00000682451.1:n.4181_4182insTCTCAAATTCTCTTGCTTTTCTATGTCCCTTTTGAATAACTTCCTCTGGGAGATTAGC (FBXO11)
ENST00000684712.1:n.4443_4444insTCTCAAATTCTCTTGCTTTTCTATGTCCCTTTTGAATAACTTCCTCTGGGAGATTAGC (FBXO11)
ENST00000234420.11:c.3916_3917insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) MANE Select ENSP00000234420.5:p.Ala1306GlyfsTer2
ENST00000540021.6:c.3526_3527insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000446475.1:p.Ala1176GlyfsTer2
ENST00000652107.1:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000498629.1:p.Ala1207GlyfsTer2
ENST00000673637.1:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000501310.1:p.Ala1207GlyfsTer2
ENST00000234420.9:c.3916_3917insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000234420.4:p.Ala1306GlyfsTer2
ENST00000405808.5:c.169+1628_169+1629insTCTCAAATTCTCTTGCTTTTCTATGTCCCTTTTGAATAACTTCCTCTGGGAGATTAGC (FBXO11) ENSP00000385127.1:n.169+1628_169+1629insTCTCAAATTCTCTTGCTTTTC...
ENST00000434234.5:c.*124+1427_*124+1428insTCTCAAATTCTCTTGCTTTTCTATGTCCCTTTTGAATAACTTCCTCTGGGAGATTAGC (FBXO11) ENSP00000402692.1:n.*124+1427_*124+1428insTCTCAAATTCTCTTGCTTT...
ENST00000445503.5:c.*3263_*3264insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000405294.1:n.*3263_*3264insGCTAATCTCCCAGAGGAAGTTATTCAA...
ENST00000538136.1:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000438580.1:p.Ala1004GlyfsTer2
ENST00000540021.5:c.3526_3527insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000446475.1:p.Ala1176GlyfsTer2
ENST00000614496.4:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000477844.1:p.Ala1004GlyfsTer2
ENST00000622629.4:c.817_818insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) ENSP00000482078.1:p.Ala273GlyfsTer2
NM_000179.2:c.3916_3917insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA , LRG_219t1:c.3916_3917insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_000170.1:p.Ala1306GlyfsTer2
NM_001281492.1:c.3526_3527insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268421.1:p.Ala1176GlyfsTer2
NM_001281493.1:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268422.1:p.Ala1004GlyfsTer2
NM_001281494.1:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268423.1:p.Ala1004GlyfsTer2
XM_005264271.1:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_005264328.1:p.Ala1207GlyfsTer2
XM_011532798.1:c.3733_3734insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_011531100.1:p.Ala1245GlyfsTer2
XM_011532799.1:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_011531101.1:p.Ala1207GlyfsTer2
XM_011532800.1:c.3619_3620insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_011531102.1:p.Ala1207GlyfsTer2
XM_024452819.1:c.4009_4010insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_024308587.1:p.Ala1337GlyfsTer2
XM_024452820.1:c.3826_3827insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_024308588.1:p.Ala1276GlyfsTer2
XM_024452821.1:c.3712_3713insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_024308589.1:p.Ala1238GlyfsTer2
XM_024452822.1:c.3103_3104insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) XP_024308590.1:p.Ala1035GlyfsTer2
NM_000179.3:c.3916_3917insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) MANE Select NP_000170.1:p.Ala1306GlyfsTer2
NM_001281492.2:c.3526_3527insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268421.1:p.Ala1176GlyfsTer2
NM_001281493.2:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268422.1:p.Ala1004GlyfsTer2
NM_001281494.2:c.3010_3011insGCTAATCTCCCAGAGGAAGTTATTCAAAAGGGACATAGAAAAGCAAGAGAATTTGAGA (MSH6) NP_001268423.1:p.Ala1004GlyfsTer2