Canonical Allele Identifier: CA2495867139

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47466496_47466500delinsCAAGT , CM000664.2:g.47466496_47466500delinsCAAGT	GRCh38
NC_000002.11:g.47693635_47693639delinsCAAGT , CM000664.1:g.47693635_47693639delinsCAAGT	GRCh37
NC_000002.10:g.47547139_47547143delinsCAAGT	NCBI36
NG_007110.2:g.68373_68377delinsCAAGT , LRG_218:g.68373_68377delinsCAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1511-162_1511-158delinsCAAGT	ENSP00000495641.2:n.1511-162_1511-158delinsCAAGT
ENST00000233146.7:c.1511-162_1511-158delinsCAAGT MANE Select	ENSP00000233146.2:n.1511-162_1511-158delinsCAAGT
ENST00000543555.6:c.1313-162_1313-158delinsCAAGT	ENSP00000442697.1:n.1313-162_1313-158delinsCAAGT
ENST00000644092.1:c.1511-162_1511-158delinsCAAGT	ENSP00000496351.1:n.1511-162_1511-158delinsCAAGT
ENST00000645339.1:c.1511-162_1511-158delinsCAAGT	ENSP00000496441.1:n.1511-162_1511-158delinsCAAGT
ENST00000645506.1:c.1511-162_1511-158delinsCAAGT	ENSP00000495455.1:n.1511-162_1511-158delinsCAAGT
ENST00000646415.1:c.1511-162_1511-158delinsCAAGT	ENSP00000495543.1:n.1511-162_1511-158delinsCAAGT
ENST00000233146.6:c.1511-162_1511-158delinsCAAGT	ENSP00000233146.2:n.1511-162_1511-158delinsCAAGT
ENST00000406134.5:c.1511-162_1511-158delinsCAAGT	ENSP00000384199.1:n.1511-162_1511-158delinsCAAGT
ENST00000543555.5:c.1313-162_1313-158delinsCAAGT	ENSP00000442697.1:n.1313-162_1313-158delinsCAAGT
ENST00000610696.4:c.1511-162_1511-158delinsCAAGT	ENSP00000483159.1:n.1511-162_1511-158delinsCAAGT
ENST00000613514.4:c.*51-162_*51-158delinsCAAGT	ENSP00000484137.1:n.*51-162_*51-158delinsCAAGT
ENST00000617333.3:c.*277-162_*277-158delinsCAAGT	ENSP00000482468.1:n.*277-162_*277-158delinsCAAGT
ENST00000617938.4:c.*483-162_*483-158delinsCAAGT	ENSP00000481158.1:n.*483-162_*483-158delinsCAAGT
ENST00000621359.2:c.1511-162_1511-158delinsCAAGT	ENSP00000481416.1:n.1511-162_1511-158delinsCAAGT
NM_000251.2:c.1511-162_1511-158delinsCAAGT , LRG_218t1:c.1511-162_1511-158delinsCAAGT	NP_000242.1:n.1511-162_1511-158delinsCAAGT
NM_001258281.1:c.1313-162_1313-158delinsCAAGT	NP_001245210.1:n.1313-162_1313-158delinsCAAGT
XM_005264332.2:c.1511-162_1511-158delinsCAAGT	XP_005264389.2:n.1511-162_1511-158delinsCAAGT
XM_011532867.1:c.1511-162_1511-158delinsCAAGT	XP_011531169.1:n.1511-162_1511-158delinsCAAGT
XR_939685.1:n.1583-162_1583-158delinsCAAGT
XM_005264332.4:c.1511-162_1511-158delinsCAAGT	XP_005264389.2:n.1511-162_1511-158delinsCAAGT
XM_011532867.2:c.1511-162_1511-158delinsCAAGT	XP_011531169.1:n.1511-162_1511-158delinsCAAGT
XR_001738747.2:n.1573-162_1573-158delinsCAAGT
XR_939685.2:n.1573-162_1573-158delinsCAAGT
NM_000251.3:c.1511-162_1511-158delinsCAAGT MANE Select	NP_000242.1:n.1511-162_1511-158delinsCAAGT