Canonical Allele Identifier: CA2496052794

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47804841_47804845delinsTAAGA , CM000664.2:g.47804841_47804845delinsTAAGA GRCh38
NC_000002.11:g.48031980_48031984delinsTAAGA , CM000664.1:g.48031980_48031984delinsTAAGA GRCh37
NC_000002.10:g.47885484_47885488delinsTAAGA NCBI36
NG_007111.1:g.26695_26699delinsTAAGA , LRG_219:g.26695_26699delinsTAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3142-69_3142-65delinsTAAGA (MSH6) ENSP00000406248.2:n.3142-69_3142-65delinsTAAGA
ENST00000420813.6:c.3142-69_3142-65delinsTAAGA (MSH6) ENSP00000390382.2:n.3142-69_3142-65delinsTAAGA
ENST00000455383.6:c.3142-69_3142-65delinsTAAGA (MSH6) ENSP00000397484.2:n.3142-69_3142-65delinsTAAGA
ENST00000700004.2:c.3173-777_3173-773delinsTAAGA (MSH6) ENSP00000514752.2:n.3173-777_3173-773delinsTAAGA
ENST00000699999.1:n.3523-69_3523-65delinsTAAGA (MSH6)
ENST00000700000.1:c.1873-69_1873-65delinsTAAGA (MSH6) ENSP00000514749.1:n.1873-69_1873-65delinsTAAGA
ENST00000700002.1:c.3445-69_3445-65delinsTAAGA (MSH6) ENSP00000514750.1:n.3445-69_3445-65delinsTAAGA
ENST00000700003.1:c.894-69_894-65delinsTAAGA (MSH6) ENSP00000514751.1:n.894-69_894-65delinsTAAGA
ENST00000700004.1:c.2330-777_2330-773delinsTAAGA (MSH6) ENSP00000514752.1:n.2330-777_2330-773delinsTAAGA
ENST00000700005.1:n.2290-69_2290-65delinsTAAGA (MSH6)
ENST00000700006.1:n.3442_3446delinsTAAGA (MSH6)
ENST00000700007.1:n.1444-69_1444-65delinsTAAGA (MSH6)
ENST00000700008.1:n.1018-69_1018-65delinsTAAGA (MSH6)
ENST00000700009.1:n.1017-69_1017-65delinsTAAGA (MSH6)
ENST00000700010.1:n.848-69_848-65delinsTAAGA (MSH6)
ENST00000700011.1:n.2074_2078delinsTAAGA (MSH6)
ENST00000234420.11:c.3439-69_3439-65delinsTAAGA (MSH6) MANE Select ENSP00000234420.5:n.3439-69_3439-65delinsTAAGA
ENST00000540021.6:c.3049-69_3049-65delinsTAAGA (MSH6) ENSP00000446475.1:n.3049-69_3049-65delinsTAAGA
ENST00000652107.1:c.3142-69_3142-65delinsTAAGA (MSH6) ENSP00000498629.1:n.3142-69_3142-65delinsTAAGA
ENST00000673637.1:c.3142-69_3142-65delinsTAAGA (MSH6) ENSP00000501310.1:n.3142-69_3142-65delinsTAAGA
ENST00000234420.9:c.3439-69_3439-65delinsTAAGA (MSH6) ENSP00000234420.4:n.3439-69_3439-65delinsTAAGA
ENST00000405808.5:c.169+3350_169+3354delinsTCTTA (FBXO11) ENSP00000385127.1:n.169+3350_169+3354delinsTCTTA
ENST00000434234.5:c.*124+3149_*124+3153delinsTCTTA (FBXO11) ENSP00000402692.1:n.*124+3149_*124+3153delinsTCTTA
ENST00000445503.5:c.*2786-69_*2786-65delinsTAAGA (MSH6) ENSP00000405294.1:n.*2786-69_*2786-65delinsTAAGA
ENST00000538136.1:c.2533-69_2533-65delinsTAAGA (MSH6) ENSP00000438580.1:n.2533-69_2533-65delinsTAAGA
ENST00000540021.5:c.3049-69_3049-65delinsTAAGA (MSH6) ENSP00000446475.1:n.3049-69_3049-65delinsTAAGA
ENST00000614496.4:c.2533-69_2533-65delinsTAAGA (MSH6) ENSP00000477844.1:n.2533-69_2533-65delinsTAAGA
ENST00000622629.4:c.335-61_335-57delinsTAAGA (MSH6) ENSP00000482078.1:n.335-61_335-57delinsTAAGA
NM_000179.2:c.3439-69_3439-65delinsTAAGA , LRG_219t1:c.3439-69_3439-65delinsTAAGA (MSH6) NP_000170.1:n.3439-69_3439-65delinsTAAGA
NM_001281492.1:c.3049-69_3049-65delinsTAAGA (MSH6) NP_001268421.1:n.3049-69_3049-65delinsTAAGA
NM_001281493.1:c.2533-69_2533-65delinsTAAGA (MSH6) NP_001268422.1:n.2533-69_2533-65delinsTAAGA
NM_001281494.1:c.2533-69_2533-65delinsTAAGA (MSH6) NP_001268423.1:n.2533-69_2533-65delinsTAAGA
XM_005264271.1:c.3142-69_3142-65delinsTAAGA (MSH6) XP_005264328.1:n.3142-69_3142-65delinsTAAGA
XM_011532798.1:c.3256-69_3256-65delinsTAAGA (MSH6) XP_011531100.1:n.3256-69_3256-65delinsTAAGA
XM_011532799.1:c.3142-69_3142-65delinsTAAGA (MSH6) XP_011531101.1:n.3142-69_3142-65delinsTAAGA
XM_011532800.1:c.3142-69_3142-65delinsTAAGA (MSH6) XP_011531102.1:n.3142-69_3142-65delinsTAAGA
XM_024452819.1:c.3439-69_3439-65delinsTAAGA (MSH6) XP_024308587.1:n.3439-69_3439-65delinsTAAGA
XM_024452820.1:c.3256-69_3256-65delinsTAAGA (MSH6) XP_024308588.1:n.3256-69_3256-65delinsTAAGA
XM_024452821.1:c.3142-69_3142-65delinsTAAGA (MSH6) XP_024308589.1:n.3142-69_3142-65delinsTAAGA
XM_024452822.1:c.2533-69_2533-65delinsTAAGA (MSH6) XP_024308590.1:n.2533-69_2533-65delinsTAAGA
NM_000179.3:c.3439-69_3439-65delinsTAAGA (MSH6) MANE Select NP_000170.1:n.3439-69_3439-65delinsTAAGA
NM_001281492.2:c.3049-69_3049-65delinsTAAGA (MSH6) NP_001268421.1:n.3049-69_3049-65delinsTAAGA
NM_001281493.2:c.2533-69_2533-65delinsTAAGA (MSH6) NP_001268422.1:n.2533-69_2533-65delinsTAAGA
NM_001281494.2:c.2533-69_2533-65delinsTAAGA (MSH6) NP_001268423.1:n.2533-69_2533-65delinsTAAGA