Canonical Allele Identifier: CA513691347
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs1405637071

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139761G>T , CM000684.2:g.20139761G>T GRCh38
NC_000022.10:g.20127284G>T , CM000684.1:g.20127284G>T GRCh37
NC_000022.9:g.18507284G>T NCBI36
NG_021420.1:g.12921G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.426G>T MANE Select ENSP00000334490.7:p.Gly142=
ENST00000320602.11:c.384+126G>T ENSP00000317804.7:n.384+126G>T
ENST00000334554.11:c.426G>T ENSP00000334490.7:p.Gly142=
ENST00000405930.3:c.426G>T ENSP00000384716.3:p.Gly142=
ENST00000436518.5:c.393G>T ENSP00000412807.1:p.Gly131=
ENST00000468112.5:n.58-856G>T
NM_001185024.1:c.426G>T NP_001171953.1:p.Gly142=
NM_013373.3:c.426G>T NP_037505.1:p.Gly142=
XM_006724239.2:c.426G>T XP_006724302.1:p.Gly142=
NM_001185024.2:c.426G>T NP_001171953.1:p.Gly142=
NM_013373.4:c.426G>T MANE Select NP_037505.1:p.Gly142=