Canonical Allele Identifier: CA2495867153

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47466516_47466517delinsCT , CM000664.2:g.47466516_47466517delinsCT	GRCh38
NC_000002.11:g.47693655_47693656delinsCT , CM000664.1:g.47693655_47693656delinsCT	GRCh37
NC_000002.10:g.47547159_47547160delinsCT	NCBI36
NG_007110.2:g.68393_68394delinsCT , LRG_218:g.68393_68394delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1511-142_1511-141delinsCT	ENSP00000495641.2:n.1511-142_1511-141delinsCT
ENST00000233146.7:c.1511-142_1511-141delinsCT MANE Select	ENSP00000233146.2:n.1511-142_1511-141delinsCT
ENST00000543555.6:c.1313-142_1313-141delinsCT	ENSP00000442697.1:n.1313-142_1313-141delinsCT
ENST00000644092.1:c.1511-142_1511-141delinsCT	ENSP00000496351.1:n.1511-142_1511-141delinsCT
ENST00000645339.1:c.1511-142_1511-141delinsCT	ENSP00000496441.1:n.1511-142_1511-141delinsCT
ENST00000645506.1:c.1511-142_1511-141delinsCT	ENSP00000495455.1:n.1511-142_1511-141delinsCT
ENST00000646415.1:c.1511-142_1511-141delinsCT	ENSP00000495543.1:n.1511-142_1511-141delinsCT
ENST00000233146.6:c.1511-142_1511-141delinsCT	ENSP00000233146.2:n.1511-142_1511-141delinsCT
ENST00000406134.5:c.1511-142_1511-141delinsCT	ENSP00000384199.1:n.1511-142_1511-141delinsCT
ENST00000543555.5:c.1313-142_1313-141delinsCT	ENSP00000442697.1:n.1313-142_1313-141delinsCT
ENST00000610696.4:c.1511-142_1511-141delinsCT	ENSP00000483159.1:n.1511-142_1511-141delinsCT
ENST00000613514.4:c.*51-142_*51-141delinsCT	ENSP00000484137.1:n.*51-142_*51-141delinsCT
ENST00000617333.3:c.*277-142_*277-141delinsCT	ENSP00000482468.1:n.*277-142_*277-141delinsCT
ENST00000617938.4:c.*483-142_*483-141delinsCT	ENSP00000481158.1:n.*483-142_*483-141delinsCT
ENST00000621359.2:c.1511-142_1511-141delinsCT	ENSP00000481416.1:n.1511-142_1511-141delinsCT
NM_000251.2:c.1511-142_1511-141delinsCT , LRG_218t1:c.1511-142_1511-141delinsCT	NP_000242.1:n.1511-142_1511-141delinsCT
NM_001258281.1:c.1313-142_1313-141delinsCT	NP_001245210.1:n.1313-142_1313-141delinsCT
XM_005264332.2:c.1511-142_1511-141delinsCT	XP_005264389.2:n.1511-142_1511-141delinsCT
XM_011532867.1:c.1511-142_1511-141delinsCT	XP_011531169.1:n.1511-142_1511-141delinsCT
XR_939685.1:n.1583-142_1583-141delinsCT
XM_005264332.4:c.1511-142_1511-141delinsCT	XP_005264389.2:n.1511-142_1511-141delinsCT
XM_011532867.2:c.1511-142_1511-141delinsCT	XP_011531169.1:n.1511-142_1511-141delinsCT
XR_001738747.2:n.1573-142_1573-141delinsCT
XR_939685.2:n.1573-142_1573-141delinsCT
NM_000251.3:c.1511-142_1511-141delinsCT MANE Select	NP_000242.1:n.1511-142_1511-141delinsCT