Canonical Allele Identifier: CA2396214269
Gene: ZDHHC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139834G= , CM000684.2:g.20139834G= GRCh38
NC_000022.10:g.20127357G= , CM000684.1:g.20127357G= GRCh37
NC_000022.9:g.18507357G= NCBI36
NG_021420.1:g.12994G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.499G= MANE Select ENSP00000334490.7:p.Gly167=
ENST00000320602.11:c.384+199G= ENSP00000317804.7:n.384+199G=
ENST00000334554.11:c.499G= ENSP00000334490.7:p.Gly167=
ENST00000405930.3:c.499G= ENSP00000384716.3:p.Gly167=
ENST00000436518.5:c.466G= ENSP00000412807.1:p.Gly156=
ENST00000468112.5:n.58-783G=
NM_001185024.1:c.499G= NP_001171953.1:p.Gly167=
NM_013373.3:c.499G= NP_037505.1:p.Gly167=
XM_006724239.2:c.499G= XP_006724302.1:p.Gly167=
NM_001185024.2:c.499G= NP_001171953.1:p.Gly167=
NM_013373.4:c.499G= MANE Select NP_037505.1:p.Gly167=