Canonical Allele Identifier: CA2495869715

Gene: MSH2

Linked Data

• dbSNP Id: rs1478761831

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47470535G>T , CM000664.2:g.47470535G>T	GRCh38
NC_000002.11:g.47697674G>T , CM000664.1:g.47697674G>T	GRCh37
NC_000002.10:g.47551178G>T	NCBI36
NG_007110.2:g.72412G>T , LRG_218:g.72412G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.1662-430G>T	ENSP00000495641.2:n.1662-430G>T
ENST00000233146.7:c.1662-430G>T MANE Select	ENSP00000233146.2:n.1662-430G>T
ENST00000543555.6:c.1464-430G>T	ENSP00000442697.1:n.1464-430G>T
ENST00000644092.1:c.1662-453G>T	ENSP00000496351.1:n.1662-453G>T
ENST00000645339.1:c.1662-430G>T	ENSP00000496441.1:n.1662-430G>T
ENST00000645506.1:c.1662-430G>T	ENSP00000495455.1:n.1662-430G>T
ENST00000646415.1:c.1662-430G>T	ENSP00000495543.1:n.1662-430G>T
ENST00000233146.6:c.1662-430G>T	ENSP00000233146.2:n.1662-430G>T
ENST00000406134.5:c.1662-430G>T	ENSP00000384199.1:n.1662-430G>T
ENST00000543555.5:c.1464-430G>T	ENSP00000442697.1:n.1464-430G>T
ENST00000610696.4:c.*58-430G>T	ENSP00000483159.1:n.*58-430G>T
ENST00000613514.4:c.*202-430G>T	ENSP00000484137.1:n.*202-430G>T
ENST00000617333.3:c.*428-430G>T	ENSP00000482468.1:n.*428-430G>T
ENST00000617938.4:c.*634-430G>T	ENSP00000481158.1:n.*634-430G>T
ENST00000621359.2:c.1662-430G>T	ENSP00000481416.1:n.1662-430G>T
NM_000251.2:c.1662-430G>T , LRG_218t1:c.1662-430G>T	NP_000242.1:n.1662-430G>T
NM_001258281.1:c.1464-430G>T	NP_001245210.1:n.1464-430G>T
XM_005264332.2:c.1662-430G>T	XP_005264389.2:n.1662-430G>T
XM_011532867.1:c.1662-430G>T	XP_011531169.1:n.1662-430G>T
XR_939685.1:n.1734-430G>T
XM_005264332.4:c.1662-430G>T	XP_005264389.2:n.1662-430G>T
XM_011532867.2:c.1662-430G>T	XP_011531169.1:n.1662-430G>T
XR_001738747.2:n.1724-430G>T
XR_939685.2:n.1724-430G>T
NM_000251.3:c.1662-430G>T MANE Select	NP_000242.1:n.1662-430G>T