Canonical Allele Identifier: CA2495877287
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47482785G= , CM000664.2:g.47482785G= GRCh38
NC_000002.11:g.47709924G= , CM000664.1:g.47709924G= GRCh37
NC_000002.10:g.47563428G= NCBI36
NG_007110.2:g.84662G= , LRG_218:g.84662G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2634+1914G= ENSP00000495641.2:n.2634+1914G=
ENST00000233146.7:c.2641G= MANE Select ENSP00000233146.2:p.Glu881=
ENST00000543555.6:c.2443G= ENSP00000442697.1:p.Glu815=
ENST00000644092.1:c.*934+1914G= ENSP00000496351.1:n.*934+1914G=
ENST00000644900.1:c.487+1914G=
ENST00000645339.1:c.2634+1914G= ENSP00000496441.1:n.2634+1914G=
ENST00000645506.1:c.2634+1914G= ENSP00000495455.1:n.2634+1914G=
ENST00000646415.1:c.2634+1914G= ENSP00000495543.1:n.2634+1914G=
ENST00000233146.6:c.2641G= ENSP00000233146.2:p.Glu881=
ENST00000406134.5:c.2634+1914G= ENSP00000384199.1:n.2634+1914G=
ENST00000461394.5:n.75+1914G=
ENST00000543555.5:c.2443G= ENSP00000442697.1:p.Glu815=
ENST00000610696.4:c.*1037G= ENSP00000483159.1:n.*1037G=
ENST00000613514.4:c.*1181G= ENSP00000484137.1:n.*1181G=
ENST00000617333.3:c.*1407G= ENSP00000482468.1:n.*1407G=
ENST00000617938.4:c.*1613G= ENSP00000481158.1:n.*1613G=
ENST00000621359.2:c.*207G= ENSP00000481416.1:n.*207G=
NM_000251.2:c.2641G= , LRG_218t1:c.2641G= NP_000242.1:p.Glu881=
NM_001258281.1:c.2443G= NP_001245210.1:p.Glu815=
XM_005264332.2:c.2634+1914G= XP_005264389.2:n.2634+1914G=
XM_011532867.1:c.2634+1914G= XP_011531169.1:n.2634+1914G=
XR_939685.1:n.2706+1914G=
XM_005264332.4:c.2634+1914G= XP_005264389.2:n.2634+1914G=
XM_011532867.2:c.2634+1914G= XP_011531169.1:n.2634+1914G=
XR_001738747.2:n.2696+1914G=
XR_939685.2:n.2696+1914G=
NM_000251.3:c.2641G= MANE Select NP_000242.1:p.Glu881=