Canonical Allele Identifier: CA2749798699

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47474939_47474940insTTTTTTTTT , CM000664.2:g.47474939_47474940insTTTTTTTTT	GRCh38
NC_000002.11:g.47702078_47702079insTTTTTTTTT , CM000664.1:g.47702078_47702079insTTTTTTTTT	GRCh37
NC_000002.10:g.47555582_47555583insTTTTTTTTT	NCBI36
NG_007110.2:g.76816_76817insTTTTTTTTT , LRG_218:g.76816_76817insTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1760-86_1760-85insTTTTTTTTT	ENSP00000495641.2:n.1760-86_1760-85insTTTTTTTTT
ENST00000233146.7:c.1760-86_1760-85insTTTTTTTTT MANE Select	ENSP00000233146.2:n.1760-86_1760-85insTTTTTTTTT
ENST00000543555.6:c.1562-86_1562-85insTTTTTTTTT	ENSP00000442697.1:n.1562-86_1562-85insTTTTTTTTT
ENST00000644092.1:c.*60-86_*60-85insTTTTTTTTT	ENSP00000496351.1:n.*60-86_*60-85insTTTTTTTTT
ENST00000645339.1:c.1760-86_1760-85insTTTTTTTTT	ENSP00000496441.1:n.1760-86_1760-85insTTTTTTTTT
ENST00000645506.1:c.1760-86_1760-85insTTTTTTTTT	ENSP00000495455.1:n.1760-86_1760-85insTTTTTTTTT
ENST00000646415.1:c.1760-86_1760-85insTTTTTTTTT	ENSP00000495543.1:n.1760-86_1760-85insTTTTTTTTT
ENST00000233146.6:c.1760-86_1760-85insTTTTTTTTT	ENSP00000233146.2:n.1760-86_1760-85insTTTTTTTTT
ENST00000406134.5:c.1760-86_1760-85insTTTTTTTTT	ENSP00000384199.1:n.1760-86_1760-85insTTTTTTTTT
ENST00000543555.5:c.1562-86_1562-85insTTTTTTTTT	ENSP00000442697.1:n.1562-86_1562-85insTTTTTTTTT
ENST00000610696.4:c.*156-86_*156-85insTTTTTTTTT	ENSP00000483159.1:n.*156-86_*156-85insTTTTTTTTT
ENST00000613514.4:c.*300-86_*300-85insTTTTTTTTT	ENSP00000484137.1:n.*300-86_*300-85insTTTTTTTTT
ENST00000617333.3:c.*526-86_*526-85insTTTTTTTTT	ENSP00000482468.1:n.*526-86_*526-85insTTTTTTTTT
ENST00000617938.4:c.*732-86_*732-85insTTTTTTTTT	ENSP00000481158.1:n.*732-86_*732-85insTTTTTTTTT
ENST00000621359.2:c.1760-86_1760-85insTTTTTTTTT	ENSP00000481416.1:n.1760-86_1760-85insTTTTTTTTT
NM_000251.2:c.1760-86_1760-85insTTTTTTTTT , LRG_218t1:c.1760-86_1760-85insTTTTTTTTT	NP_000242.1:n.1760-86_1760-85insTTTTTTTTT
NM_001258281.1:c.1562-86_1562-85insTTTTTTTTT	NP_001245210.1:n.1562-86_1562-85insTTTTTTTTT
XM_005264332.2:c.1760-86_1760-85insTTTTTTTTT	XP_005264389.2:n.1760-86_1760-85insTTTTTTTTT
XM_011532867.1:c.1760-86_1760-85insTTTTTTTTT	XP_011531169.1:n.1760-86_1760-85insTTTTTTTTT
XR_939685.1:n.1832-86_1832-85insTTTTTTTTT
XM_005264332.4:c.1760-86_1760-85insTTTTTTTTT	XP_005264389.2:n.1760-86_1760-85insTTTTTTTTT
XM_011532867.2:c.1760-86_1760-85insTTTTTTTTT	XP_011531169.1:n.1760-86_1760-85insTTTTTTTTT
XR_001738747.2:n.1822-86_1822-85insTTTTTTTTT
XR_939685.2:n.1822-86_1822-85insTTTTTTTTT
NM_000251.3:c.1760-86_1760-85insTTTTTTTTT MANE Select	NP_000242.1:n.1760-86_1760-85insTTTTTTTTT