Canonical Allele Identifier: CA2495873396
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476385A= , CM000664.2:g.47476385A= GRCh38
NC_000002.11:g.47703524A= , CM000664.1:g.47703524A= GRCh37
NC_000002.10:g.47557028A= NCBI36
NG_007110.2:g.78262A= , LRG_218:g.78262A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2024A= ENSP00000495641.2:p.Lys675=
ENST00000233146.7:c.2024A= MANE Select ENSP00000233146.2:p.Lys675=
ENST00000543555.6:c.1826A= ENSP00000442697.1:p.Lys609=
ENST00000644092.1:c.*324A= ENSP00000496351.1:n.*324A=
ENST00000645339.1:c.2024A= ENSP00000496441.1:p.Lys675=
ENST00000645506.1:c.2024A= ENSP00000495455.1:p.Lys675=
ENST00000646415.1:c.2024A= ENSP00000495543.1:p.Lys675=
ENST00000233146.6:c.2024A= ENSP00000233146.2:p.Lys675=
ENST00000406134.5:c.2024A= ENSP00000384199.1:p.Lys675=
ENST00000543555.5:c.1826A= ENSP00000442697.1:p.Lys609=
ENST00000610696.4:c.*420A= ENSP00000483159.1:n.*420A=
ENST00000613514.4:c.*564A= ENSP00000484137.1:n.*564A=
ENST00000617333.3:c.*790A= ENSP00000482468.1:n.*790A=
ENST00000617938.4:c.*996A= ENSP00000481158.1:n.*996A=
ENST00000621359.2:c.2024A= ENSP00000481416.1:p.Lys675=
NM_000251.2:c.2024A= , LRG_218t1:c.2024A= NP_000242.1:p.Lys675=
NM_001258281.1:c.1826A= NP_001245210.1:p.Lys609=
XM_005264332.2:c.2024A= XP_005264389.2:p.Lys675=
XM_011532867.1:c.2024A= XP_011531169.1:p.Lys675=
XR_939685.1:n.2096A=
XM_005264332.4:c.2024A= XP_005264389.2:p.Lys675=
XM_011532867.2:c.2024A= XP_011531169.1:p.Lys675=
XR_001738747.2:n.2086A=
XR_939685.2:n.2086A=
NM_000251.3:c.2024A= MANE Select NP_000242.1:p.Lys675=