Canonical Allele Identifier: CA16617588

Gene: MSH2

Linked Data

• ClinVar Variation Id: 419601
• ClinVar RCV Id: RCV000479480 ; RCV000551068 ; RCV000766532 ; RCV000581059 ; RCV003470543 ; RCV004002307
• dbSNP Id: rs1064793981
• gnomAD v4: 2-47475030-G-A
• MyVariant Identifiers: chr2:g.47702169G>A (hg19) ; chr2:g.47475030G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475030G>A , CM000664.2:g.47475030G>A	GRCh38
NC_000002.11:g.47702169G>A , CM000664.1:g.47702169G>A	GRCh37
NC_000002.10:g.47555673G>A	NCBI36
NG_007110.2:g.76907G>A , LRG_218:g.76907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1765G>A	ENSP00000495641.2:p.Val589Ile
ENST00000233146.7:c.1765G>A MANE Select	ENSP00000233146.2:p.Val589Ile
ENST00000543555.6:c.1567G>A	ENSP00000442697.1:p.Val523Ile
ENST00000644092.1:c.*65G>A	ENSP00000496351.1:n.*65G>A
ENST00000645339.1:c.1765G>A	ENSP00000496441.1:p.Val589Ile
ENST00000645506.1:c.1765G>A	ENSP00000495455.1:p.Val589Ile
ENST00000646415.1:c.1765G>A	ENSP00000495543.1:p.Val589Ile
ENST00000233146.6:c.1765G>A	ENSP00000233146.2:p.Val589Ile
ENST00000406134.5:c.1765G>A	ENSP00000384199.1:p.Val589Ile
ENST00000543555.5:c.1567G>A	ENSP00000442697.1:p.Val523Ile
ENST00000610696.4:c.*161G>A	ENSP00000483159.1:n.*161G>A
ENST00000613514.4:c.*305G>A	ENSP00000484137.1:n.*305G>A
ENST00000617333.3:c.*531G>A	ENSP00000482468.1:n.*531G>A
ENST00000617938.4:c.*737G>A	ENSP00000481158.1:n.*737G>A
ENST00000621359.2:c.1765G>A	ENSP00000481416.1:p.Val589Ile
NM_000251.2:c.1765G>A , LRG_218t1:c.1765G>A	NP_000242.1:p.Val589Ile
NM_001258281.1:c.1567G>A	NP_001245210.1:p.Val523Ile
XM_005264332.2:c.1765G>A	XP_005264389.2:p.Val589Ile
XM_011532867.1:c.1765G>A	XP_011531169.1:p.Val589Ile
XR_939685.1:n.1837G>A
XM_005264332.4:c.1765G>A	XP_005264389.2:p.Val589Ile
XM_011532867.2:c.1765G>A	XP_011531169.1:p.Val589Ile
XR_001738747.2:n.1827G>A
XR_939685.2:n.1827G>A
NM_000251.3:c.1765G>A MANE Select	NP_000242.1:p.Val589Ile