Canonical Allele Identifier: CA2495834038
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47414408_47414409delinsAC , CM000664.2:g.47414408_47414409delinsAC GRCh38
NC_000002.11:g.47641547_47641548delinsAC , CM000664.1:g.47641547_47641548delinsAC GRCh37
NC_000002.10:g.47495051_47495052delinsAC NCBI36
NG_007110.2:g.16285_16286delinsAC , LRG_218:g.16285_16286delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.932_933delinsAC ENSP00000495641.2:p.Asn311=
ENST00000233146.7:c.932_933delinsAC MANE Select ENSP00000233146.2:p.Asn311=
ENST00000543555.6:c.734_735delinsAC ENSP00000442697.1:p.Asn245=
ENST00000644092.1:c.932_933delinsAC ENSP00000496351.1:p.Asn311=
ENST00000645339.1:c.932_933delinsAC ENSP00000496441.1:p.Asn311=
ENST00000645506.1:c.932_933delinsAC ENSP00000495455.1:p.Asn311=
ENST00000646415.1:c.932_933delinsAC ENSP00000495543.1:p.Asn311=
ENST00000233146.6:c.932_933delinsAC ENSP00000233146.2:p.Asn311=
ENST00000406134.5:c.932_933delinsAC ENSP00000384199.1:p.Asn311=
ENST00000543555.5:c.734_735delinsAC ENSP00000442697.1:p.Asn245=
ENST00000610696.4:c.932_933delinsAC ENSP00000483159.1:p.Asn311=
ENST00000613514.4:c.932_933delinsAC ENSP00000484137.1:p.Asn311=
ENST00000617333.3:c.932_933delinsAC ENSP00000482468.1:p.Asn311=
ENST00000617938.4:c.932_933delinsAC ENSP00000481158.1:p.Asn311=
ENST00000621359.2:c.932_933delinsAC ENSP00000481416.1:p.Asn311=
NM_000251.2:c.932_933delinsAC , LRG_218t1:c.932_933delinsAC NP_000242.1:p.Asn311=
NM_001258281.1:c.734_735delinsAC NP_001245210.1:p.Asn245=
XM_005264332.2:c.932_933delinsAC XP_005264389.2:p.Asn311=
XM_011532867.1:c.932_933delinsAC XP_011531169.1:p.Asn311=
XR_939685.1:n.1004_1005delinsAC
XM_005264332.4:c.932_933delinsAC XP_005264389.2:p.Asn311=
XM_011532867.2:c.932_933delinsAC XP_011531169.1:p.Asn311=
XR_001738747.2:n.994_995delinsAC
XR_939685.2:n.994_995delinsAC
NM_000251.3:c.932_933delinsAC MANE Select NP_000242.1:p.Asn311=