Canonical Allele Identifier: CA360346789
Gene: MSH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873119C>G , CM000667.2:g.80873119C>G GRCh38
NC_000005.9:g.80168938C>G , CM000667.1:g.80168938C>G GRCh37
NC_000005.8:g.80204694C>G NCBI36
NG_016607.1:g.223645C>G
NG_016607.2:g.223645C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3134C>G MANE Select ENSP00000265081.6:p.Ala1045Gly
ENST00000658259.1:c.2966C>G ENSP00000499617.1:p.Ala989Gly
ENST00000659302.1:c.542C>G
ENST00000667069.1:c.2939C>G ENSP00000499502.1:p.Ala980Gly
ENST00000670357.1:c.*458C>G ENSP00000499791.1:n.*458C>G
ENST00000265081.6:c.3134C>G ENSP00000265081.6:p.Ala1045Gly
NM_002439.4:c.3134C>G NP_002430.3:p.Ala1045Gly
NM_002439.5:c.3134C>G MANE Select NP_002430.3:p.Ala1045Gly