Canonical Allele Identifier: CA410734390

Gene: ZDHHC8

Linked Data

• MyVariant Identifiers: chr22:g.20127367A>C (hg19) ; chr22:g.20139844A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139844A>C , CM000684.2:g.20139844A>C	GRCh38
NC_000022.10:g.20127367A>C , CM000684.1:g.20127367A>C	GRCh37
NC_000022.9:g.18507367A>C	NCBI36
NG_021420.1:g.13004A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334554.12:c.509A>C MANE Select	ENSP00000334490.7:p.Tyr170Ser
ENST00000320602.11:c.384+209A>C	ENSP00000317804.7:n.384+209A>C
ENST00000334554.11:c.509A>C	ENSP00000334490.7:p.Tyr170Ser
ENST00000405930.3:c.509A>C	ENSP00000384716.3:p.Tyr170Ser
ENST00000436518.5:c.476A>C	ENSP00000412807.1:p.Tyr159Ser
ENST00000468112.5:n.58-773A>C
NM_001185024.1:c.509A>C	NP_001171953.1:p.Tyr170Ser
NM_013373.3:c.509A>C	NP_037505.1:p.Tyr170Ser
XM_006724239.2:c.509A>C	XP_006724302.1:p.Tyr170Ser
NM_001185024.2:c.509A>C	NP_001171953.1:p.Tyr170Ser
NM_013373.4:c.509A>C MANE Select	NP_037505.1:p.Tyr170Ser