Canonical Allele Identifier: CA2495872484

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475144A= , CM000664.2:g.47475144A=	GRCh38
NC_000002.11:g.47702283A= , CM000664.1:g.47702283A=	GRCh37
NC_000002.10:g.47555787A=	NCBI36
NG_007110.2:g.77021A= , LRG_218:g.77021A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1879A=	ENSP00000495641.2:p.Lys627=
ENST00000233146.7:c.1879A= MANE Select	ENSP00000233146.2:p.Lys627=
ENST00000543555.6:c.1681A=	ENSP00000442697.1:p.Lys561=
ENST00000644092.1:c.*179A=	ENSP00000496351.1:n.*179A=
ENST00000645339.1:c.1879A=	ENSP00000496441.1:p.Lys627=
ENST00000645506.1:c.1879A=	ENSP00000495455.1:p.Lys627=
ENST00000646415.1:c.1879A=	ENSP00000495543.1:p.Lys627=
ENST00000233146.6:c.1879A=	ENSP00000233146.2:p.Lys627=
ENST00000406134.5:c.1879A=	ENSP00000384199.1:p.Lys627=
ENST00000543555.5:c.1681A=	ENSP00000442697.1:p.Lys561=
ENST00000610696.4:c.*275A=	ENSP00000483159.1:n.*275A=
ENST00000613514.4:c.*419A=	ENSP00000484137.1:n.*419A=
ENST00000617333.3:c.*645A=	ENSP00000482468.1:n.*645A=
ENST00000617938.4:c.*851A=	ENSP00000481158.1:n.*851A=
ENST00000621359.2:c.1879A=	ENSP00000481416.1:p.Lys627=
NM_000251.2:c.1879A= , LRG_218t1:c.1879A=	NP_000242.1:p.Lys627=
NM_001258281.1:c.1681A=	NP_001245210.1:p.Lys561=
XM_005264332.2:c.1879A=	XP_005264389.2:p.Lys627=
XM_011532867.1:c.1879A=	XP_011531169.1:p.Lys627=
XR_939685.1:n.1951A=
XM_005264332.4:c.1879A=	XP_005264389.2:p.Lys627=
XM_011532867.2:c.1879A=	XP_011531169.1:p.Lys627=
XR_001738747.2:n.1941A=
XR_939685.2:n.1941A=
NM_000251.3:c.1879A= MANE Select	NP_000242.1:p.Lys627=