Canonical Allele Identifier: CA2495834153

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414530_47414533delinsATAT , CM000664.2:g.47414530_47414533delinsATAT	GRCh38
NC_000002.11:g.47641669_47641672delinsATAT , CM000664.1:g.47641669_47641672delinsATAT	GRCh37
NC_000002.10:g.47495173_47495176delinsATAT	NCBI36
NG_007110.2:g.16407_16410delinsATAT , LRG_218:g.16407_16410delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.942+112_942+115delinsATAT	ENSP00000495641.2:n.942+112_942+115delinsATAT
ENST00000233146.7:c.942+112_942+115delinsATAT MANE Select	ENSP00000233146.2:n.942+112_942+115delinsATAT
ENST00000543555.6:c.744+112_744+115delinsATAT	ENSP00000442697.1:n.744+112_744+115delinsATAT
ENST00000644092.1:c.942+112_942+115delinsATAT	ENSP00000496351.1:n.942+112_942+115delinsATAT
ENST00000645339.1:c.942+112_942+115delinsATAT	ENSP00000496441.1:n.942+112_942+115delinsATAT
ENST00000645506.1:c.942+112_942+115delinsATAT	ENSP00000495455.1:n.942+112_942+115delinsATAT
ENST00000646415.1:c.942+112_942+115delinsATAT	ENSP00000495543.1:n.942+112_942+115delinsATAT
ENST00000233146.6:c.942+112_942+115delinsATAT	ENSP00000233146.2:n.942+112_942+115delinsATAT
ENST00000406134.5:c.942+112_942+115delinsATAT	ENSP00000384199.1:n.942+112_942+115delinsATAT
ENST00000543555.5:c.744+112_744+115delinsATAT	ENSP00000442697.1:n.744+112_744+115delinsATAT
ENST00000610696.4:c.942+112_942+115delinsATAT	ENSP00000483159.1:n.942+112_942+115delinsATAT
ENST00000613514.4:c.942+112_942+115delinsATAT	ENSP00000484137.1:n.942+112_942+115delinsATAT
ENST00000617333.3:c.942+112_942+115delinsATAT	ENSP00000482468.1:n.942+112_942+115delinsATAT
ENST00000617938.4:c.942+112_942+115delinsATAT	ENSP00000481158.1:n.942+112_942+115delinsATAT
ENST00000621359.2:c.942+112_942+115delinsATAT	ENSP00000481416.1:n.942+112_942+115delinsATAT
NM_000251.2:c.942+112_942+115delinsATAT , LRG_218t1:c.942+112_942+115delinsATAT	NP_000242.1:n.942+112_942+115delinsATAT
NM_001258281.1:c.744+112_744+115delinsATAT	NP_001245210.1:n.744+112_744+115delinsATAT
XM_005264332.2:c.942+112_942+115delinsATAT	XP_005264389.2:n.942+112_942+115delinsATAT
XM_011532867.1:c.942+112_942+115delinsATAT	XP_011531169.1:n.942+112_942+115delinsATAT
XR_939685.1:n.1014+112_1014+115delinsATAT
XM_005264332.4:c.942+112_942+115delinsATAT	XP_005264389.2:n.942+112_942+115delinsATAT
XM_011532867.2:c.942+112_942+115delinsATAT	XP_011531169.1:n.942+112_942+115delinsATAT
XR_001738747.2:n.1004+112_1004+115delinsATAT
XR_939685.2:n.1004+112_1004+115delinsATAT
NM_000251.3:c.942+112_942+115delinsATAT MANE Select	NP_000242.1:n.942+112_942+115delinsATAT