Canonical Allele Identifier: CA346729077

Gene: MSH2

Linked Data

• ClinVar Variation Id: 843335
• ClinVar RCV Id: RCV001045938 ; RCV001189187
• dbSNP Id: rs1558519495
• gnomAD v4: 2-47476369-C-A
• MyVariant Identifiers: chr2:g.47703508C>A (hg19) ; chr2:g.47476369C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476369C>A , CM000664.2:g.47476369C>A	GRCh38
NC_000002.11:g.47703508C>A , CM000664.1:g.47703508C>A	GRCh37
NC_000002.10:g.47557012C>A	NCBI36
NG_007110.2:g.78246C>A , LRG_218:g.78246C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2008C>A	ENSP00000495641.2:p.Pro670Thr
ENST00000233146.7:c.2008C>A MANE Select	ENSP00000233146.2:p.Pro670Thr
ENST00000543555.6:c.1810C>A	ENSP00000442697.1:p.Pro604Thr
ENST00000644092.1:c.*308C>A	ENSP00000496351.1:n.*308C>A
ENST00000645339.1:c.2008C>A	ENSP00000496441.1:p.Pro670Thr
ENST00000645506.1:c.2008C>A	ENSP00000495455.1:p.Pro670Thr
ENST00000646415.1:c.2008C>A	ENSP00000495543.1:p.Pro670Thr
ENST00000233146.6:c.2008C>A	ENSP00000233146.2:p.Pro670Thr
ENST00000406134.5:c.2008C>A	ENSP00000384199.1:p.Pro670Thr
ENST00000543555.5:c.1810C>A	ENSP00000442697.1:p.Pro604Thr
ENST00000610696.4:c.*404C>A	ENSP00000483159.1:n.*404C>A
ENST00000613514.4:c.*548C>A	ENSP00000484137.1:n.*548C>A
ENST00000617333.3:c.*774C>A	ENSP00000482468.1:n.*774C>A
ENST00000617938.4:c.*980C>A	ENSP00000481158.1:n.*980C>A
ENST00000621359.2:c.2008C>A	ENSP00000481416.1:p.Pro670Thr
NM_000251.2:c.2008C>A , LRG_218t1:c.2008C>A	NP_000242.1:p.Pro670Thr
NM_001258281.1:c.1810C>A	NP_001245210.1:p.Pro604Thr
XM_005264332.2:c.2008C>A	XP_005264389.2:p.Pro670Thr
XM_011532867.1:c.2008C>A	XP_011531169.1:p.Pro670Thr
XR_939685.1:n.2080C>A
XM_005264332.4:c.2008C>A	XP_005264389.2:p.Pro670Thr
XM_011532867.2:c.2008C>A	XP_011531169.1:p.Pro670Thr
XR_001738747.2:n.2070C>A
XR_939685.2:n.2070C>A
NM_000251.3:c.2008C>A MANE Select	NP_000242.1:p.Pro670Thr