Canonical Allele Identifier: CA915943901

Gene: MSH2

Linked Data

• ClinVar Variation Id: 638998
• ClinVar RCV Id: RCV000791687
• dbSNP Id: rs1573484581

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47429811_47429813del , CM000664.2:g.47429811_47429813del	GRCh38
NC_000002.11:g.47656950_47656952del , CM000664.1:g.47656950_47656952del	GRCh37
NC_000002.10:g.47510454_47510456del	NCBI36
NG_007110.2:g.31688_31690del , LRG_218:g.31688_31690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1146_1148del	ENSP00000495641.2:p.Arg383del
ENST00000233146.7:c.1146_1148del MANE Select	ENSP00000233146.2:p.Arg383del
ENST00000543555.6:c.948_950del	ENSP00000442697.1:p.Arg317del
ENST00000644092.1:c.1146_1148del	ENSP00000496351.1:p.Arg383del
ENST00000645339.1:c.1146_1148del	ENSP00000496441.1:p.Arg383del
ENST00000645506.1:c.1146_1148del	ENSP00000495455.1:p.Arg383del
ENST00000646415.1:c.1146_1148del	ENSP00000495543.1:p.Arg383del
ENST00000233146.6:c.1146_1148del	ENSP00000233146.2:p.Arg383del
ENST00000406134.5:c.1146_1148del	ENSP00000384199.1:p.Arg383del
ENST00000543555.5:c.948_950del	ENSP00000442697.1:p.Arg317del
ENST00000610696.4:c.1146_1148del	ENSP00000483159.1:p.Arg383del
ENST00000613514.4:c.1146_1148del	ENSP00000484137.1:p.Arg383del
ENST00000617333.3:c.1145_1147del	ENSP00000482468.1:p.Val382del
ENST00000617938.4:c.*118_*120del	ENSP00000481158.1:n.*118_*120del
ENST00000621359.2:c.1146_1148del	ENSP00000481416.1:p.Arg383del
NM_000251.2:c.1146_1148del , LRG_218t1:c.1146_1148del	NP_000242.1:p.Arg383del
NM_001258281.1:c.948_950del	NP_001245210.1:p.Arg317del
XM_005264332.2:c.1146_1148del	XP_005264389.2:p.Arg383del
XM_011532867.1:c.1146_1148del	XP_011531169.1:p.Arg383del
XR_939685.1:n.1218_1220del
XM_005264332.4:c.1146_1148del	XP_005264389.2:p.Arg383del
XM_011532867.2:c.1146_1148del	XP_011531169.1:p.Arg383del
XR_001738747.2:n.1208_1210del
XR_939685.2:n.1208_1210del
NM_000251.3:c.1146_1148del MANE Select	NP_000242.1:p.Arg383del