Canonical Allele Identifier: CA2495867282
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47466706G= , CM000664.2:g.47466706G= GRCh38
NC_000002.11:g.47693845G= , CM000664.1:g.47693845G= GRCh37
NC_000002.10:g.47547349G= NCBI36
NG_007110.2:g.68583G= , LRG_218:g.68583G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.1559G= ENSP00000495641.2:p.Gly520=
ENST00000233146.7:c.1559G= MANE Select ENSP00000233146.2:p.Gly520=
ENST00000543555.6:c.1361G= ENSP00000442697.1:p.Gly454=
ENST00000644092.1:c.1559G= ENSP00000496351.1:p.Gly520=
ENST00000645339.1:c.1559G= ENSP00000496441.1:p.Gly520=
ENST00000645506.1:c.1559G= ENSP00000495455.1:p.Gly520=
ENST00000646415.1:c.1559G= ENSP00000495543.1:p.Gly520=
ENST00000233146.6:c.1559G= ENSP00000233146.2:p.Gly520=
ENST00000406134.5:c.1559G= ENSP00000384199.1:p.Gly520=
ENST00000543555.5:c.1361G= ENSP00000442697.1:p.Gly454=
ENST00000610696.4:c.1559G= ENSP00000483159.1:p.Gly520=
ENST00000613514.4:c.*99G= ENSP00000484137.1:n.*99G=
ENST00000617333.3:c.*325G= ENSP00000482468.1:n.*325G=
ENST00000617938.4:c.*531G= ENSP00000481158.1:n.*531G=
ENST00000621359.2:c.1559G= ENSP00000481416.1:p.Gly520=
NM_000251.2:c.1559G= , LRG_218t1:c.1559G= NP_000242.1:p.Gly520=
NM_001258281.1:c.1361G= NP_001245210.1:p.Gly454=
XM_005264332.2:c.1559G= XP_005264389.2:p.Gly520=
XM_011532867.1:c.1559G= XP_011531169.1:p.Gly520=
XR_939685.1:n.1631G=
XM_005264332.4:c.1559G= XP_005264389.2:p.Gly520=
XM_011532867.2:c.1559G= XP_011531169.1:p.Gly520=
XR_001738747.2:n.1621G=
XR_939685.2:n.1621G=
NM_000251.3:c.1559G= MANE Select NP_000242.1:p.Gly520=