Canonical Allele Identifier: CA410734169

Gene: ZDHHC8

Linked Data

• MyVariant Identifiers: chr22:g.20127276T>A (hg19) ; chr22:g.20139753T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139753T>A , CM000684.2:g.20139753T>A	GRCh38
NC_000022.10:g.20127276T>A , CM000684.1:g.20127276T>A	GRCh37
NC_000022.9:g.18507276T>A	NCBI36
NG_021420.1:g.12913T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.418T>A MANE Select	ENSP00000334490.7:p.Cys140Ser
ENST00000320602.11:c.384+118T>A	ENSP00000317804.7:n.384+118T>A
ENST00000334554.11:c.418T>A	ENSP00000334490.7:p.Cys140Ser
ENST00000405930.3:c.418T>A	ENSP00000384716.3:p.Cys140Ser
ENST00000436518.5:c.385T>A	ENSP00000412807.1:p.Cys129Ser
ENST00000468112.5:n.58-864T>A
NM_001185024.1:c.418T>A	NP_001171953.1:p.Cys140Ser
NM_013373.3:c.418T>A	NP_037505.1:p.Cys140Ser
XM_006724239.2:c.418T>A	XP_006724302.1:p.Cys140Ser
NM_001185024.2:c.418T>A	NP_001171953.1:p.Cys140Ser
NM_013373.4:c.418T>A MANE Select	NP_037505.1:p.Cys140Ser