Canonical Allele Identifier: CA2655369088

Gene: ZDHHC8

Linked Data

• gnomAD v4: 22-20139828-GCCTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139829_20139833del , CM000684.2:g.20139829_20139833del	GRCh38
NC_000022.10:g.20127352_20127356del , CM000684.1:g.20127352_20127356del	GRCh37
NC_000022.9:g.18507352_18507356del	NCBI36
NG_021420.1:g.12989_12993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.494_498del MANE Select	ENSP00000334490.7:p.Ala165GlyfsTer10
ENST00000320602.11:c.384+194_384+198del	ENSP00000317804.7:n.384+194_384+198del
ENST00000334554.11:c.494_498del	ENSP00000334490.7:p.Ala165GlyfsTer10
ENST00000405930.3:c.494_498del	ENSP00000384716.3:p.Ala165GlyfsTer10
ENST00000436518.5:c.461_465del	ENSP00000412807.1:p.Ala154GlyfsTer10
ENST00000468112.5:n.58-788_58-784del
NM_001185024.1:c.494_498del	NP_001171953.1:p.Ala165GlyfsTer10
NM_013373.3:c.494_498del	NP_037505.1:p.Ala165GlyfsTer10
XM_006724239.2:c.494_498del	XP_006724302.1:p.Ala165GlyfsTer10
NM_001185024.2:c.494_498del	NP_001171953.1:p.Ala165GlyfsTer10
NM_013373.4:c.494_498del MANE Select	NP_037505.1:p.Ala165GlyfsTer10