Canonical Allele Identifier: CA445225434
Gene: MSH3 HGNC NCBI

Linked Data

gnomAD v4: 5-80873129-A-G
MyVariant Identifiers: chr5:g.80168948A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873129A>G , CM000667.2:g.80873129A>G GRCh38
NC_000005.9:g.80168948A>G , CM000667.1:g.80168948A>G GRCh37
NC_000005.8:g.80204704A>G NCBI36
NG_016607.1:g.223655A>G
NG_016607.2:g.223655A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3144A>G MANE Select ENSP00000265081.6:p.Gln1048=
ENST00000658259.1:c.2976A>G ENSP00000499617.1:p.Gln992=
ENST00000659302.1:c.552A>G
ENST00000667069.1:c.2949A>G ENSP00000499502.1:p.Gln983=
ENST00000670357.1:c.*468A>G ENSP00000499791.1:n.*468A>G
ENST00000265081.6:c.3144A>G ENSP00000265081.6:p.Gln1048=
NM_002439.4:c.3144A>G NP_002430.3:p.Gln1048=
NM_002439.5:c.3144A>G MANE Select NP_002430.3:p.Gln1048=