Canonical Allele Identifier: CA10108575
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs777211797

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.499G>A MANE Select ENSP00000334490.7:p.Gly167Ser
ENST00000320602.11:c.384+199G>A ENSP00000317804.7:n.384+199G>A
ENST00000334554.11:c.499G>A ENSP00000334490.7:p.Gly167Ser
ENST00000405930.3:c.499G>A ENSP00000384716.3:p.Gly167Ser
ENST00000436518.5:c.466G>A ENSP00000412807.1:p.Gly156Ser
ENST00000468112.5:n.58-783G>A
NM_001185024.1:c.499G>A NP_001171953.1:p.Gly167Ser
NM_013373.3:c.499G>A NP_037505.1:p.Gly167Ser
XM_006724239.2:c.499G>A XP_006724302.1:p.Gly167Ser
NM_001185024.2:c.499G>A NP_001171953.1:p.Gly167Ser
NM_013373.4:c.499G>A MANE Select NP_037505.1:p.Gly167Ser