Canonical Allele Identifier: CA2495833985
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47414342_47414347delinsTTGAAC , CM000664.2:g.47414342_47414347delinsTTGAAC GRCh38
NC_000002.11:g.47641481_47641486delinsTTGAAC , CM000664.1:g.47641481_47641486delinsTTGAAC GRCh37
NC_000002.10:g.47494985_47494990delinsTTGAAC NCBI36
NG_007110.2:g.16219_16224delinsTTGAAC , LRG_218:g.16219_16224delinsTTGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.866_871delinsTTGAAC ENSP00000495641.2:p.Phe289=
ENST00000233146.7:c.866_871delinsTTGAAC MANE Select ENSP00000233146.2:p.Phe289=
ENST00000543555.6:c.668_673delinsTTGAAC ENSP00000442697.1:p.Phe223=
ENST00000644092.1:c.866_871delinsTTGAAC ENSP00000496351.1:p.Phe289=
ENST00000645339.1:c.866_871delinsTTGAAC ENSP00000496441.1:p.Phe289=
ENST00000645506.1:c.866_871delinsTTGAAC ENSP00000495455.1:p.Phe289=
ENST00000646415.1:c.866_871delinsTTGAAC ENSP00000495543.1:p.Phe289=
ENST00000233146.6:c.866_871delinsTTGAAC ENSP00000233146.2:p.Phe289=
ENST00000406134.5:c.866_871delinsTTGAAC ENSP00000384199.1:p.Phe289=
ENST00000543555.5:c.668_673delinsTTGAAC ENSP00000442697.1:p.Phe223=
ENST00000610696.4:c.866_871delinsTTGAAC ENSP00000483159.1:p.Phe289=
ENST00000613514.4:c.866_871delinsTTGAAC ENSP00000484137.1:p.Phe289=
ENST00000617333.3:c.866_871delinsTTGAAC ENSP00000482468.1:p.Phe289=
ENST00000617938.4:c.866_871delinsTTGAAC ENSP00000481158.1:p.Phe289=
ENST00000621359.2:c.866_871delinsTTGAAC ENSP00000481416.1:p.Phe289=
NM_000251.2:c.866_871delinsTTGAAC , LRG_218t1:c.866_871delinsTTGAAC NP_000242.1:p.Phe289=
NM_001258281.1:c.668_673delinsTTGAAC NP_001245210.1:p.Phe223=
XM_005264332.2:c.866_871delinsTTGAAC XP_005264389.2:p.Phe289=
XM_011532867.1:c.866_871delinsTTGAAC XP_011531169.1:p.Phe289=
XR_939685.1:n.938_943delinsTTGAAC
XM_005264332.4:c.866_871delinsTTGAAC XP_005264389.2:p.Phe289=
XM_011532867.2:c.866_871delinsTTGAAC XP_011531169.1:p.Phe289=
XR_001738747.2:n.928_933delinsTTGAAC
XR_939685.2:n.928_933delinsTTGAAC
NM_000251.3:c.866_871delinsTTGAAC MANE Select NP_000242.1:p.Phe289=