Canonical Allele Identifier: CA2495877288

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482789A= , CM000664.2:g.47482789A=	GRCh38
NC_000002.11:g.47709928A= , CM000664.1:g.47709928A=	GRCh37
NC_000002.10:g.47563432A=	NCBI36
NG_007110.2:g.84666A= , LRG_218:g.84666A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2634+1918A=	ENSP00000495641.2:n.2634+1918A=
ENST00000233146.7:c.2645A= MANE Select	ENSP00000233146.2:p.Lys882=
ENST00000543555.6:c.2447A=	ENSP00000442697.1:p.Lys816=
ENST00000644092.1:c.*934+1918A=	ENSP00000496351.1:n.*934+1918A=
ENST00000644900.1:c.487+1918A=
ENST00000645339.1:c.2634+1918A=	ENSP00000496441.1:n.2634+1918A=
ENST00000645506.1:c.2634+1918A=	ENSP00000495455.1:n.2634+1918A=
ENST00000646415.1:c.2634+1918A=	ENSP00000495543.1:n.2634+1918A=
ENST00000233146.6:c.2645A=	ENSP00000233146.2:p.Lys882=
ENST00000406134.5:c.2634+1918A=	ENSP00000384199.1:n.2634+1918A=
ENST00000461394.5:n.75+1918A=
ENST00000543555.5:c.2447A=	ENSP00000442697.1:p.Lys816=
ENST00000610696.4:c.*1041A=	ENSP00000483159.1:n.*1041A=
ENST00000613514.4:c.*1185A=	ENSP00000484137.1:n.*1185A=
ENST00000617333.3:c.*1411A=	ENSP00000482468.1:n.*1411A=
ENST00000617938.4:c.*1617A=	ENSP00000481158.1:n.*1617A=
ENST00000621359.2:c.*211A=	ENSP00000481416.1:n.*211A=
NM_000251.2:c.2645A= , LRG_218t1:c.2645A=	NP_000242.1:p.Lys882=
NM_001258281.1:c.2447A=	NP_001245210.1:p.Lys816=
XM_005264332.2:c.2634+1918A=	XP_005264389.2:n.2634+1918A=
XM_011532867.1:c.2634+1918A=	XP_011531169.1:n.2634+1918A=
XR_939685.1:n.2706+1918A=
XM_005264332.4:c.2634+1918A=	XP_005264389.2:n.2634+1918A=
XM_011532867.2:c.2634+1918A=	XP_011531169.1:n.2634+1918A=
XR_001738747.2:n.2696+1918A=
XR_939685.2:n.2696+1918A=
NM_000251.3:c.2645A= MANE Select	NP_000242.1:p.Lys882=