Canonical Allele Identifier: CA3006927
Gene: HERC5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10516809

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88499935A>G , CM000666.2:g.88499935A>G GRCh38
NC_000004.11:g.89421086A>G , CM000666.1:g.89421086A>G GRCh37
NC_000004.10:g.89640109A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_016323.3:c.2454A>G VV NP_057407.2:p.Gln818=
XM_011532022.1:c.2229A>G XP_011530324.1:p.Gln743=
XM_011532023.1:c.2166A>G XP_011530325.1:p.Gln722=
XM_011532022.2:c.2682A>G XP_011530324.2:p.Gln894=
NM_016323.4:c.2454A>G VV MANE Preferred NP_057407.2:p.Gln818=
ENST00000264350.7:c.2454A>G ENSP00000264350.3:p.Gln818=
ENST00000502913.1:n.1175A>G
ENST00000508159.1:c.1368A>G ENSP00000424129.1:p.Gln456=
ENST00000510223.5:n.1942A>G