Canonical Allele Identifier: CA360346794
Gene: MSH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873122C>G , CM000667.2:g.80873122C>G GRCh38
NC_000005.9:g.80168941C>G , CM000667.1:g.80168941C>G GRCh37
NC_000005.8:g.80204697C>G NCBI36
NG_016607.1:g.223648C>G
NG_016607.2:g.223648C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3137C>G MANE Select ENSP00000265081.6:p.Ala1046Gly
ENST00000658259.1:c.2969C>G ENSP00000499617.1:p.Ala990Gly
ENST00000659302.1:c.545C>G
ENST00000667069.1:c.2942C>G ENSP00000499502.1:p.Ala981Gly
ENST00000670357.1:c.*461C>G ENSP00000499791.1:n.*461C>G
ENST00000265081.6:c.3137C>G ENSP00000265081.6:p.Ala1046Gly
NM_002439.4:c.3137C>G NP_002430.3:p.Ala1046Gly
NM_002439.5:c.3137C>G MANE Select NP_002430.3:p.Ala1046Gly