Canonical Allele Identifier: CA346730065

Gene: MSH2

Linked Data

• dbSNP Id: rs1558521964
• MyVariant Identifiers: chr2:g.47705572C>A (hg19) ; chr2:g.47478433C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478433C>A , CM000664.2:g.47478433C>A	GRCh38
NC_000002.11:g.47705572C>A , CM000664.1:g.47705572C>A	GRCh37
NC_000002.10:g.47559076C>A	NCBI36
NG_007110.2:g.80310C>A , LRG_218:g.80310C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2372C>A	ENSP00000495641.2:p.Ala791Asp
ENST00000233146.7:c.2372C>A MANE Select	ENSP00000233146.2:p.Ala791Asp
ENST00000543555.6:c.2174C>A	ENSP00000442697.1:p.Ala725Asp
ENST00000644092.1:c.*672C>A	ENSP00000496351.1:n.*672C>A
ENST00000644900.1:c.225C>A
ENST00000645339.1:c.2372C>A	ENSP00000496441.1:p.Ala791Asp
ENST00000645506.1:c.2372C>A	ENSP00000495455.1:p.Ala791Asp
ENST00000646415.1:c.2372C>A	ENSP00000495543.1:p.Ala791Asp
ENST00000233146.6:c.2372C>A	ENSP00000233146.2:p.Ala791Asp
ENST00000406134.5:c.2372C>A	ENSP00000384199.1:p.Ala791Asp
ENST00000543555.5:c.2174C>A	ENSP00000442697.1:p.Ala725Asp
ENST00000610696.4:c.*768C>A	ENSP00000483159.1:n.*768C>A
ENST00000613514.4:c.*912C>A	ENSP00000484137.1:n.*912C>A
ENST00000617333.3:c.*1138C>A	ENSP00000482468.1:n.*1138C>A
ENST00000617938.4:c.*1344C>A	ENSP00000481158.1:n.*1344C>A
ENST00000621359.2:c.2371C>A	ENSP00000481416.1:p.Pro791Thr
NM_000251.2:c.2372C>A , LRG_218t1:c.2372C>A	NP_000242.1:p.Ala791Asp
NM_001258281.1:c.2174C>A	NP_001245210.1:p.Ala725Asp
XM_005264332.2:c.2372C>A	XP_005264389.2:p.Ala791Asp
XM_011532867.1:c.2372C>A	XP_011531169.1:p.Ala791Asp
XR_939685.1:n.2444C>A
XM_005264332.4:c.2372C>A	XP_005264389.2:p.Ala791Asp
XM_011532867.2:c.2372C>A	XP_011531169.1:p.Ala791Asp
XR_001738747.2:n.2434C>A
XR_939685.2:n.2434C>A
NM_000251.3:c.2372C>A MANE Select	NP_000242.1:p.Ala791Asp