Canonical Allele Identifier: CA10108531

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs757280778
• ExAC: 22:20127041 G / A
• gnomAD v2: 22-20127041-G-A
• gnomAD v3: 22-20139518-G-A
• gnomAD v4: 22-20139518-G-A
• MyVariant Identifiers: chr22:g.20127041G>A (hg19) ; chr22:g.20139518G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139518G>A , CM000684.2:g.20139518G>A	GRCh38
NC_000022.10:g.20127041G>A , CM000684.1:g.20127041G>A	GRCh37
NC_000022.9:g.18507041G>A	NCBI36
NG_021420.1:g.12678G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.267G>A MANE Select	ENSP00000334490.7:p.Pro89=
ENST00000320602.11:c.267G>A	ENSP00000317804.7:p.Pro89=
ENST00000334554.11:c.267G>A	ENSP00000334490.7:p.Pro89=
ENST00000405930.3:c.267G>A	ENSP00000384716.3:p.Pro89=
ENST00000436518.5:c.234G>A	ENSP00000412807.1:p.Pro78=
ENST00000468112.5:n.58-1099G>A
NM_001185024.1:c.267G>A	NP_001171953.1:p.Pro89=
NM_013373.3:c.267G>A	NP_037505.1:p.Pro89=
XM_006724239.2:c.267G>A	XP_006724302.1:p.Pro89=
NM_001185024.2:c.267G>A	NP_001171953.1:p.Pro89=
NM_013373.4:c.267G>A MANE Select	NP_037505.1:p.Pro89=