Canonical Allele Identifier: CA2396214268
Gene: ZDHHC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139833C= , CM000684.2:g.20139833C= GRCh38
NC_000022.10:g.20127356C= , CM000684.1:g.20127356C= GRCh37
NC_000022.9:g.18507356C= NCBI36
NG_021420.1:g.12993C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.498C= MANE Select ENSP00000334490.7:p.Phe166=
ENST00000320602.11:c.384+198C= ENSP00000317804.7:n.384+198C=
ENST00000334554.11:c.498C= ENSP00000334490.7:p.Phe166=
ENST00000405930.3:c.498C= ENSP00000384716.3:p.Phe166=
ENST00000436518.5:c.465C= ENSP00000412807.1:p.Phe155=
ENST00000468112.5:n.58-784C=
NM_001185024.1:c.498C= NP_001171953.1:p.Phe166=
NM_013373.3:c.498C= NP_037505.1:p.Phe166=
XM_006724239.2:c.498C= XP_006724302.1:p.Phe166=
NM_001185024.2:c.498C= NP_001171953.1:p.Phe166=
NM_013373.4:c.498C= MANE Select NP_037505.1:p.Phe166=