Canonical Allele Identifier: CA346734855

Gene: MSH6

Linked Data

• ClinVar Variation Id: 1727867
• ClinVar RCV Id: RCV002320499
• MyVariant Identifiers: chr2:g.48010484C>A (hg19) ; chr2:g.47783345C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783345C>A , CM000664.2:g.47783345C>A	GRCh38
NC_000002.11:g.48010484C>A , CM000664.1:g.48010484C>A	GRCh37
NC_000002.10:g.47863988C>A	NCBI36
NG_007111.1:g.5199C>A , LRG_219:g.5199C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.112C>A	ENSP00000514752.2:p.Pro38Thr
ENST00000699999.1:n.196C>A
ENST00000700000.1:c.112C>A	ENSP00000514749.1:p.Pro38Thr
ENST00000700001.1:n.184C>A
ENST00000700002.1:c.112C>A	ENSP00000514750.1:p.Pro38Thr
ENST00000700003.1:c.112C>A	ENSP00000514751.1:p.Pro38Thr
ENST00000234420.11:c.112C>A MANE Select	ENSP00000234420.5:p.Pro38Thr
ENST00000540021.6:c.112C>A	ENSP00000446475.1:p.Pro38Thr
ENST00000652107.1:c.-37-7582C>A	ENSP00000498629.1:n.-37-7582C>A
ENST00000673637.1:c.-38+114C>A	ENSP00000501310.1:n.-38+114C>A
ENST00000673922.1:n.201C>A
ENST00000234420.9:c.112C>A	ENSP00000234420.4:p.Pro38Thr
ENST00000445503.5:c.112C>A	ENSP00000405294.1:p.Pro38Thr
ENST00000456246.1:c.112C>A	ENSP00000410570.1:p.Pro38Thr
ENST00000493177.1:n.176C>A
ENST00000540021.5:c.112C>A	ENSP00000446475.1:p.Pro38Thr
ENST00000606499.1:c.-37-7582C>A	ENSP00000475605.1:n.-37-7582C>A
ENST00000614496.4:c.-625C>A	ENSP00000477844.1:n.-625C>A
ENST00000616033.4:c.110C>A	ENSP00000480261.1:p.Pro37His
ENST00000622629.4:c.-2985C>A	ENSP00000482078.1:n.-2985C>A
NM_000179.2:c.112C>A , LRG_219t1:c.112C>A	NP_000170.1:p.Pro38Thr
NM_001281492.1:c.112C>A	NP_001268421.1:p.Pro38Thr
NM_001281493.1:c.-625C>A	NP_001268422.1:n.-625C>A
XM_011532800.1:c.-38+114C>A	XP_011531102.1:n.-38+114C>A
XM_024452819.1:c.112C>A	XP_024308587.1:p.Pro38Thr
XM_024452822.1:c.-625C>A	XP_024308590.1:n.-625C>A
NM_000179.3:c.112C>A MANE Select	NP_000170.1:p.Pro38Thr
NM_001281492.2:c.112C>A	NP_001268421.1:p.Pro38Thr
NM_001281493.2:c.-625C>A	NP_001268422.1:n.-625C>A