Canonical Allele Identifier: CA2832539647

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414448_47414449insA , CM000664.2:g.47414448_47414449insA	GRCh38
NC_000002.11:g.47641587_47641588insA , CM000664.1:g.47641587_47641588insA	GRCh37
NC_000002.10:g.47495091_47495092insA	NCBI36
NG_007110.2:g.16325_16326insA , LRG_218:g.16325_16326insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.942+30_942+31insA	ENSP00000495641.2:n.942+30_942+31insA
ENST00000233146.7:c.942+30_942+31insA MANE Select	ENSP00000233146.2:n.942+30_942+31insA
ENST00000543555.6:c.744+30_744+31insA	ENSP00000442697.1:n.744+30_744+31insA
ENST00000644092.1:c.942+30_942+31insA	ENSP00000496351.1:n.942+30_942+31insA
ENST00000645339.1:c.942+30_942+31insA	ENSP00000496441.1:n.942+30_942+31insA
ENST00000645506.1:c.942+30_942+31insA	ENSP00000495455.1:n.942+30_942+31insA
ENST00000646415.1:c.942+30_942+31insA	ENSP00000495543.1:n.942+30_942+31insA
ENST00000233146.6:c.942+30_942+31insA	ENSP00000233146.2:n.942+30_942+31insA
ENST00000406134.5:c.942+30_942+31insA	ENSP00000384199.1:n.942+30_942+31insA
ENST00000543555.5:c.744+30_744+31insA	ENSP00000442697.1:n.744+30_744+31insA
ENST00000610696.4:c.942+30_942+31insA	ENSP00000483159.1:n.942+30_942+31insA
ENST00000613514.4:c.942+30_942+31insA	ENSP00000484137.1:n.942+30_942+31insA
ENST00000617333.3:c.942+30_942+31insA	ENSP00000482468.1:n.942+30_942+31insA
ENST00000617938.4:c.942+30_942+31insA	ENSP00000481158.1:n.942+30_942+31insA
ENST00000621359.2:c.942+30_942+31insA	ENSP00000481416.1:n.942+30_942+31insA
NM_000251.2:c.942+30_942+31insA , LRG_218t1:c.942+30_942+31insA	NP_000242.1:n.942+30_942+31insA
NM_001258281.1:c.744+30_744+31insA	NP_001245210.1:n.744+30_744+31insA
XM_005264332.2:c.942+30_942+31insA	XP_005264389.2:n.942+30_942+31insA
XM_011532867.1:c.942+30_942+31insA	XP_011531169.1:n.942+30_942+31insA
XR_939685.1:n.1014+30_1014+31insA
XM_005264332.4:c.942+30_942+31insA	XP_005264389.2:n.942+30_942+31insA
XM_011532867.2:c.942+30_942+31insA	XP_011531169.1:n.942+30_942+31insA
XR_001738747.2:n.1004+30_1004+31insA
XR_939685.2:n.1004+30_1004+31insA
NM_000251.3:c.942+30_942+31insA MANE Select	NP_000242.1:n.942+30_942+31insA