Canonical Allele Identifier: CA2495865213

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47463038_47463039delinsAC , CM000664.2:g.47463038_47463039delinsAC	GRCh38
NC_000002.11:g.47690177_47690178delinsAC , CM000664.1:g.47690177_47690178delinsAC	GRCh37
NC_000002.10:g.47543681_47543682delinsAC	NCBI36
NG_007110.2:g.64915_64916delinsAC , LRG_218:g.64915_64916delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1394_1395delinsAC	ENSP00000495641.2:p.Asn465=
ENST00000233146.7:c.1394_1395delinsAC MANE Select	ENSP00000233146.2:p.Asn465=
ENST00000543555.6:c.1196_1197delinsAC	ENSP00000442697.1:p.Asn399=
ENST00000644092.1:c.1394_1395delinsAC	ENSP00000496351.1:p.Asn465=
ENST00000645339.1:c.1394_1395delinsAC	ENSP00000496441.1:p.Asn465=
ENST00000645506.1:c.1394_1395delinsAC	ENSP00000495455.1:p.Asn465=
ENST00000646415.1:c.1394_1395delinsAC	ENSP00000495543.1:p.Asn465=
ENST00000233146.6:c.1394_1395delinsAC	ENSP00000233146.2:p.Asn465=
ENST00000406134.5:c.1394_1395delinsAC	ENSP00000384199.1:p.Asn465=
ENST00000543555.5:c.1196_1197delinsAC	ENSP00000442697.1:p.Asn399=
ENST00000610696.4:c.1394_1395delinsAC	ENSP00000483159.1:p.Asn465=
ENST00000613514.4:c.1394_1395delinsAC	ENSP00000484137.1:p.Asn465=
ENST00000617333.3:c.*160_*161delinsAC	ENSP00000482468.1:n.*160_*161delinsAC
ENST00000617938.4:c.*366_*367delinsAC	ENSP00000481158.1:n.*366_*367delinsAC
ENST00000621359.2:c.1394_1395delinsAC	ENSP00000481416.1:p.Asn465=
NM_000251.2:c.1394_1395delinsAC , LRG_218t1:c.1394_1395delinsAC	NP_000242.1:p.Asn465=
NM_001258281.1:c.1196_1197delinsAC	NP_001245210.1:p.Asn399=
XM_005264332.2:c.1394_1395delinsAC	XP_005264389.2:p.Asn465=
XM_011532867.1:c.1394_1395delinsAC	XP_011531169.1:p.Asn465=
XR_939685.1:n.1466_1467delinsAC
XM_005264332.4:c.1394_1395delinsAC	XP_005264389.2:p.Asn465=
XM_011532867.2:c.1394_1395delinsAC	XP_011531169.1:p.Asn465=
XR_001738747.2:n.1456_1457delinsAC
XR_939685.2:n.1456_1457delinsAC
NM_000251.3:c.1394_1395delinsAC MANE Select	NP_000242.1:p.Asn465=