Canonical Allele Identifier: CA513691278

Gene: ZDHHC8

Linked Data

• MyVariant Identifiers: chr22:g.20127395A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139872A>C , CM000684.2:g.20139872A>C	GRCh38
NC_000022.10:g.20127395A>C , CM000684.1:g.20127395A>C	GRCh37
NC_000022.9:g.18507395A>C	NCBI36
NG_021420.1:g.13032A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.537A>C MANE Select	ENSP00000334490.7:p.Gly179=
ENST00000320602.11:c.384+237A>C	ENSP00000317804.7:n.384+237A>C
ENST00000334554.11:c.537A>C	ENSP00000334490.7:p.Gly179=
ENST00000405930.3:c.537A>C	ENSP00000384716.3:p.Gly179=
ENST00000436518.5:c.504A>C	ENSP00000412807.1:p.Gly168=
ENST00000468112.5:n.58-745A>C
NM_001185024.1:c.537A>C	NP_001171953.1:p.Gly179=
NM_013373.3:c.537A>C	NP_037505.1:p.Gly179=
XM_006724239.2:c.537A>C	XP_006724302.1:p.Gly179=
NM_001185024.2:c.537A>C	NP_001171953.1:p.Gly179=
NM_013373.4:c.537A>C MANE Select	NP_037505.1:p.Gly179=