Canonical Allele Identifier: CA10108576

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs752095710
• ExAC: 22:20127359 C / T
• gnomAD v2: 22-20127359-C-T
• gnomAD v4: 22-20139836-C-T
• MyVariant Identifiers: chr22:g.20127359C>T (hg19) ; chr22:g.20139836C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139836C>T , CM000684.2:g.20139836C>T	GRCh38
NC_000022.10:g.20127359C>T , CM000684.1:g.20127359C>T	GRCh37
NC_000022.9:g.18507359C>T	NCBI36
NG_021420.1:g.12996C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.501C>T MANE Select	ENSP00000334490.7:p.Gly167=
ENST00000320602.11:c.384+201C>T	ENSP00000317804.7:n.384+201C>T
ENST00000334554.11:c.501C>T	ENSP00000334490.7:p.Gly167=
ENST00000405930.3:c.501C>T	ENSP00000384716.3:p.Gly167=
ENST00000436518.5:c.468C>T	ENSP00000412807.1:p.Gly156=
ENST00000468112.5:n.58-781C>T
NM_001185024.1:c.501C>T	NP_001171953.1:p.Gly167=
NM_013373.3:c.501C>T	NP_037505.1:p.Gly167=
XM_006724239.2:c.501C>T	XP_006724302.1:p.Gly167=
NM_001185024.2:c.501C>T	NP_001171953.1:p.Gly167=
NM_013373.4:c.501C>T MANE Select	NP_037505.1:p.Gly167=