Canonical Allele Identifier: CA1558564200
Gene: MSH3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3137C= MANE Select ENSP00000265081.6:p.Ala1046=
ENST00000658259.1:c.2969C= ENSP00000499617.1:p.Ala990=
ENST00000659302.1:c.545C=
ENST00000667069.1:c.2942C= ENSP00000499502.1:p.Ala981=
ENST00000670357.1:c.*461C= ENSP00000499791.1:n.*461C=
ENST00000265081.6:c.3137C= ENSP00000265081.6:p.Ala1046=
NM_002439.4:c.3137C= NP_002430.3:p.Ala1046=
NM_002439.5:c.3137C= MANE Select NP_002430.3:p.Ala1046=