Canonical Allele Identifier: CA2495874682
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47478528T= , CM000664.2:g.47478528T= GRCh38
NC_000002.11:g.47705667T= , CM000664.1:g.47705667T= GRCh37
NC_000002.10:g.47559171T= NCBI36
NG_007110.2:g.80405T= , LRG_218:g.80405T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2458+9T= ENSP00000495641.2:n.2458+9T=
ENST00000233146.7:c.2458+9T= MANE Select ENSP00000233146.2:n.2458+9T=
ENST00000543555.6:c.2260+9T= ENSP00000442697.1:n.2260+9T=
ENST00000644092.1:c.*758+9T= ENSP00000496351.1:n.*758+9T=
ENST00000644900.1:c.311+9T=
ENST00000645339.1:c.2458+9T= ENSP00000496441.1:n.2458+9T=
ENST00000645506.1:c.2458+9T= ENSP00000495455.1:n.2458+9T=
ENST00000646415.1:c.2458+9T= ENSP00000495543.1:n.2458+9T=
ENST00000233146.6:c.2458+9T= ENSP00000233146.2:n.2458+9T=
ENST00000406134.5:c.2458+9T= ENSP00000384199.1:n.2458+9T=
ENST00000543555.5:c.2260+9T= ENSP00000442697.1:n.2260+9T=
ENST00000610696.4:c.*854+9T= ENSP00000483159.1:n.*854+9T=
ENST00000613514.4:c.*998+9T= ENSP00000484137.1:n.*998+9T=
ENST00000617333.3:c.*1224+9T= ENSP00000482468.1:n.*1224+9T=
ENST00000617938.4:c.*1430+9T= ENSP00000481158.1:n.*1430+9T=
ENST00000621359.2:c.*24+9T= ENSP00000481416.1:n.*24+9T=
NM_000251.2:c.2458+9T= , LRG_218t1:c.2458+9T= NP_000242.1:n.2458+9T=
NM_001258281.1:c.2260+9T= NP_001245210.1:n.2260+9T=
XM_005264332.2:c.2458+9T= XP_005264389.2:n.2458+9T=
XM_011532867.1:c.2458+9T= XP_011531169.1:n.2458+9T=
XR_939685.1:n.2530+9T=
XM_005264332.4:c.2458+9T= XP_005264389.2:n.2458+9T=
XM_011532867.2:c.2458+9T= XP_011531169.1:n.2458+9T=
XR_001738747.2:n.2520+9T=
XR_939685.2:n.2520+9T=
NM_000251.3:c.2458+9T= MANE Select NP_000242.1:n.2458+9T=