Canonical Allele Identifier: CA2496052933

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47804992_47804995delinsTTAC , CM000664.2:g.47804992_47804995delinsTTAC GRCh38
NC_000002.11:g.48032131_48032134delinsTTAC , CM000664.1:g.48032131_48032134delinsTTAC GRCh37
NC_000002.10:g.47885635_47885638delinsTTAC NCBI36
NG_007111.1:g.26846_26849delinsTTAC , LRG_219:g.26846_26849delinsTTAC
NG_008397.1:g.105681_105684delinsGTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3224_3227delinsTTAC (MSH6) ENSP00000406248.2:p.Phe1075=
ENST00000420813.6:c.3224_3227delinsTTAC (MSH6) ENSP00000390382.2:p.Phe1075=
ENST00000455383.6:c.3224_3227delinsTTAC (MSH6) ENSP00000397484.2:p.Phe1075=
ENST00000700004.2:c.3173-626_3173-623delinsTTAC (MSH6) ENSP00000514752.2:n.3173-626_3173-623deli...
ENST00000699999.1:n.3605_3608delinsTTAC (MSH6)
ENST00000700000.1:c.1955_1958delinsTTAC (MSH6) ENSP00000514749.1:p.Phe652=
ENST00000700002.1:c.3527_3530delinsTTAC (MSH6) ENSP00000514750.1:p.Phe1176=
ENST00000700003.1:c.976_979delinsTTAC (MSH6) ENSP00000514751.1:n.976_979delinsTTAC
ENST00000700004.1:c.2330-626_2330-623delinsTTAC (MSH6) ENSP00000514752.1:n.2330-626_2330-623deli...
ENST00000700005.1:n.2372_2375delinsTTAC (MSH6)
ENST00000700006.1:n.3593_3596delinsTTAC (MSH6)
ENST00000700007.1:n.1526_1529delinsTTAC (MSH6)
ENST00000700008.1:n.1100_1103delinsTTAC (MSH6)
ENST00000700009.1:n.1099_1102delinsTTAC (MSH6)
ENST00000700010.1:n.930_933delinsTTAC (MSH6)
ENST00000700011.1:n.2225_2228delinsTTAC (MSH6)
ENST00000234420.11:c.3521_3524delinsTTAC (MSH6) MANE Select ENSP00000234420.5:p.Phe1174=
ENST00000540021.6:c.3131_3134delinsTTAC (MSH6) ENSP00000446475.1:p.Phe1044=
ENST00000652107.1:c.3224_3227delinsTTAC (MSH6) ENSP00000498629.1:p.Phe1075=
ENST00000673637.1:c.3224_3227delinsTTAC (MSH6) ENSP00000501310.1:p.Phe1075=
ENST00000234420.9:c.3521_3524delinsTTAC (MSH6) ENSP00000234420.4:p.Phe1174=
ENST00000405808.5:c.169+3200_169+3203delinsGTAA (FBXO11) ENSP00000385127.1:n.169+3200_169+3203deli...
ENST00000434234.5:c.*124+2999_*124+3002delinsGTAA (FBXO11) ENSP00000402692.1:n.*124+2999_*124+3002de...
ENST00000445503.5:c.*2868_*2871delinsTTAC (MSH6) ENSP00000405294.1:n.*2868_*2871delinsTTAC...
ENST00000538136.1:c.2615_2618delinsTTAC (MSH6) ENSP00000438580.1:p.Phe872=
ENST00000540021.5:c.3131_3134delinsTTAC (MSH6) ENSP00000446475.1:p.Phe1044=
ENST00000614496.4:c.2615_2618delinsTTAC (MSH6) ENSP00000477844.1:p.Phe872=
ENST00000622629.4:c.425_428delinsTTAC (MSH6) ENSP00000482078.1:p.Phe142=
NM_000179.2:c.3521_3524delinsTTAC , LRG_219t1:c.3521_3524delinsTTAC (MSH6) NP_000170.1:p.Phe1174=
NM_001281492.1:c.3131_3134delinsTTAC (MSH6) NP_001268421.1:p.Phe1044=
NM_001281493.1:c.2615_2618delinsTTAC (MSH6) NP_001268422.1:p.Phe872=
NM_001281494.1:c.2615_2618delinsTTAC (MSH6) NP_001268423.1:p.Phe872=
XM_005264271.1:c.3224_3227delinsTTAC (MSH6) XP_005264328.1:p.Phe1075=
XM_011532798.1:c.3338_3341delinsTTAC (MSH6) XP_011531100.1:p.Phe1113=
XM_011532799.1:c.3224_3227delinsTTAC (MSH6) XP_011531101.1:p.Phe1075=
XM_011532800.1:c.3224_3227delinsTTAC (MSH6) XP_011531102.1:p.Phe1075=
XM_024452819.1:c.3521_3524delinsTTAC (MSH6) XP_024308587.1:p.Phe1174=
XM_024452820.1:c.3338_3341delinsTTAC (MSH6) XP_024308588.1:p.Phe1113=
XM_024452821.1:c.3224_3227delinsTTAC (MSH6) XP_024308589.1:p.Phe1075=
XM_024452822.1:c.2615_2618delinsTTAC (MSH6) XP_024308590.1:p.Phe872=
NM_000179.3:c.3521_3524delinsTTAC (MSH6) MANE Select NP_000170.1:p.Phe1174=
NM_001281492.2:c.3131_3134delinsTTAC (MSH6) NP_001268421.1:p.Phe1044=
NM_001281493.2:c.2615_2618delinsTTAC (MSH6) NP_001268422.1:p.Phe872=
NM_001281494.2:c.2615_2618delinsTTAC (MSH6) NP_001268423.1:p.Phe872=