Canonical Allele Identifier: CA658823249
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 548796
ClinVar RCV Id: RCV000662770
dbSNP Id: rs1553408127

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783288del , CM000664.2:g.47783288del GRCh38
NC_000002.11:g.48010427del , CM000664.1:g.48010427del GRCh37
NC_000002.10:g.47863931del NCBI36
NG_007111.1:g.5142del , LRG_219:g.5142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700004.2:c.55del ENSP00000514752.2:p.Asp19MetfsTer?
ENST00000699999.1:n.139del
ENST00000700000.1:c.55del ENSP00000514749.1:p.Asp19MetfsTer?
ENST00000700001.1:n.127del
ENST00000700002.1:c.55del ENSP00000514750.1:p.Asp19MetfsTer?
ENST00000700003.1:c.55del ENSP00000514751.1:p.Asp19MetfsTer?
ENST00000234420.11:c.55del MANE Select ENSP00000234420.5:p.Asp19MetfsTer?
ENST00000540021.6:c.55del ENSP00000446475.1:p.Asp19MetfsTer?
ENST00000652107.1:c.-37-7639del ENSP00000498629.1:n.-37-7639del
ENST00000673637.1:c.-38+57del ENSP00000501310.1:n.-38+57del
ENST00000673922.1:n.144del
ENST00000234420.9:c.55del ENSP00000234420.4:p.Asp19MetfsTer?
ENST00000445503.5:c.55del ENSP00000405294.1:p.Asp19MetfsTer?
ENST00000456246.1:c.55del ENSP00000410570.1:p.Asp19MetfsTer?
ENST00000493177.1:n.119del
ENST00000540021.5:c.55del ENSP00000446475.1:p.Asp19MetfsTer?
ENST00000606499.1:c.-37-7639del ENSP00000475605.1:n.-37-7639del
ENST00000614496.4:c.-682del ENSP00000477844.1:n.-682del
ENST00000616033.4:c.55del ENSP00000480261.1:p.Asp19MetfsTer?
ENST00000622629.4:c.-3042del ENSP00000482078.1:n.-3042del
NM_000179.2:c.55del , LRG_219t1:c.55del NP_000170.1:p.Asp19MetfsTer?
NM_001281492.1:c.55del NP_001268421.1:p.Asp19MetfsTer?
NM_001281493.1:c.-682del NP_001268422.1:n.-682del
XM_011532800.1:c.-38+57del XP_011531102.1:n.-38+57del
XM_024452819.1:c.55del XP_024308587.1:p.Asp19MetfsTer?
XM_024452822.1:c.-682del XP_024308590.1:n.-682del
NM_000179.3:c.55del MANE Select NP_000170.1:p.Asp19MetfsTer?
NM_001281492.2:c.55del NP_001268421.1:p.Asp19MetfsTer?
NM_001281493.2:c.-682del NP_001268422.1:n.-682del