Canonical Allele Identifier: CA916080254
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 846087
ClinVar RCV Id: RCV001049297
dbSNP Id: rs1668118988

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783330del , CM000664.2:g.47783330del GRCh38
NC_000002.11:g.48010469del , CM000664.1:g.48010469del GRCh37
NC_000002.10:g.47863973del NCBI36
NG_007111.1:g.5184del , LRG_219:g.5184del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700004.2:c.97del ENSP00000514752.2:p.Arg33ValfsTer?
ENST00000699999.1:n.181del
ENST00000700000.1:c.97del ENSP00000514749.1:p.Arg33ValfsTer?
ENST00000700001.1:n.169del
ENST00000700002.1:c.97del ENSP00000514750.1:p.Arg33ValfsTer?
ENST00000700003.1:c.97del ENSP00000514751.1:p.Arg33ValfsTer?
ENST00000234420.11:c.97del MANE Select ENSP00000234420.5:p.Arg33ValfsTer?
ENST00000540021.6:c.97del ENSP00000446475.1:p.Arg33ValfsTer?
ENST00000652107.1:c.-37-7597del ENSP00000498629.1:n.-37-7597del
ENST00000673637.1:c.-38+99del ENSP00000501310.1:n.-38+99del
ENST00000673922.1:n.186del
ENST00000234420.9:c.97del ENSP00000234420.4:p.Arg33ValfsTer?
ENST00000445503.5:c.97del ENSP00000405294.1:p.Arg33ValfsTer?
ENST00000456246.1:c.97del ENSP00000410570.1:p.Arg33ValfsTer?
ENST00000493177.1:n.161del
ENST00000540021.5:c.97del ENSP00000446475.1:p.Arg33ValfsTer?
ENST00000606499.1:c.-37-7597del ENSP00000475605.1:n.-37-7597del
ENST00000614496.4:c.-640del ENSP00000477844.1:n.-640del
ENST00000616033.4:c.97del ENSP00000480261.1:p.Arg33ValfsTer?
ENST00000622629.4:c.-3000del ENSP00000482078.1:n.-3000del
NM_000179.2:c.97del , LRG_219t1:c.97del NP_000170.1:p.Arg33ValfsTer?
NM_001281492.1:c.97del NP_001268421.1:p.Arg33ValfsTer?
NM_001281493.1:c.-640del NP_001268422.1:n.-640del
XM_011532800.1:c.-38+99del XP_011531102.1:n.-38+99del
XM_024452819.1:c.97del XP_024308587.1:p.Arg33ValfsTer?
XM_024452822.1:c.-640del XP_024308590.1:n.-640del
NM_000179.3:c.97del MANE Select NP_000170.1:p.Arg33ValfsTer?
NM_001281492.2:c.97del NP_001268421.1:p.Arg33ValfsTer?
NM_001281493.2:c.-640del NP_001268422.1:n.-640del