Canonical Allele Identifier: CA2495843384

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47429384_47429392delinsGGCATGATC , CM000664.2:g.47429384_47429392delinsGGCATGATC	GRCh38
NC_000002.11:g.47656523_47656531delinsGGCATGATC , CM000664.1:g.47656523_47656531delinsGGCATGATC	GRCh37
NC_000002.10:g.47510027_47510035delinsGGCATGATC	NCBI36
NG_007110.2:g.31261_31269delinsGGCATGATC , LRG_218:g.31261_31269delinsGGCATGATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1077-358_1077-350delinsGGCATGATC	ENSP00000495641.2:n.1077-358_1077-350delinsGGCATGATC
ENST00000233146.7:c.1077-358_1077-350delinsGGCATGATC MANE Select	ENSP00000233146.2:n.1077-358_1077-350delinsGGCATGATC
ENST00000543555.6:c.879-358_879-350delinsGGCATGATC	ENSP00000442697.1:n.879-358_879-350delinsGGCATGATC
ENST00000644092.1:c.1077-358_1077-350delinsGGCATGATC	ENSP00000496351.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000645339.1:c.1077-358_1077-350delinsGGCATGATC	ENSP00000496441.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000645506.1:c.1077-358_1077-350delinsGGCATGATC	ENSP00000495455.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000646415.1:c.1077-358_1077-350delinsGGCATGATC	ENSP00000495543.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000233146.6:c.1077-358_1077-350delinsGGCATGATC	ENSP00000233146.2:n.1077-358_1077-350delinsGGCATGATC
ENST00000406134.5:c.1077-358_1077-350delinsGGCATGATC	ENSP00000384199.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000543555.5:c.879-358_879-350delinsGGCATGATC	ENSP00000442697.1:n.879-358_879-350delinsGGCATGATC
ENST00000610696.4:c.1077-358_1077-350delinsGGCATGATC	ENSP00000483159.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000613514.4:c.1077-358_1077-350delinsGGCATGATC	ENSP00000484137.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000617333.3:c.1077-358_1077-350delinsGGCATGATC	ENSP00000482468.1:n.1077-358_1077-350delinsGGCATGATC
ENST00000617938.4:c.*49-358_*49-350delinsGGCATGATC	ENSP00000481158.1:n.*49-358_*49-350delinsGGCATGATC
ENST00000621359.2:c.1077-358_1077-350delinsGGCATGATC	ENSP00000481416.1:n.1077-358_1077-350delinsGGCATGATC
NM_000251.2:c.1077-358_1077-350delinsGGCATGATC , LRG_218t1:c.1077-358_1077-350delinsGGCATGATC	NP_000242.1:n.1077-358_1077-350delinsGGCATGATC
NM_001258281.1:c.879-358_879-350delinsGGCATGATC	NP_001245210.1:n.879-358_879-350delinsGGCATGATC
XM_005264332.2:c.1077-358_1077-350delinsGGCATGATC	XP_005264389.2:n.1077-358_1077-350delinsGGCATGATC
XM_011532867.1:c.1077-358_1077-350delinsGGCATGATC	XP_011531169.1:n.1077-358_1077-350delinsGGCATGATC
XR_939685.1:n.1149-358_1149-350delinsGGCATGATC
XM_005264332.4:c.1077-358_1077-350delinsGGCATGATC	XP_005264389.2:n.1077-358_1077-350delinsGGCATGATC
XM_011532867.2:c.1077-358_1077-350delinsGGCATGATC	XP_011531169.1:n.1077-358_1077-350delinsGGCATGATC
XR_001738747.2:n.1139-358_1139-350delinsGGCATGATC
XR_939685.2:n.1139-358_1139-350delinsGGCATGATC
NM_000251.3:c.1077-358_1077-350delinsGGCATGATC MANE Select	NP_000242.1:n.1077-358_1077-350delinsGGCATGATC