Canonical Allele Identifier: CA10108578

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs374648833
• ExAC: 22:20127369 G / A
• gnomAD v2: 22-20127369-G-A
• gnomAD v3: 22-20139846-G-A
• gnomAD v4: 22-20139846-G-A
• MyVariant Identifiers: chr22:g.20127369G>A (hg19) ; chr22:g.20139846G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139846G>A , CM000684.2:g.20139846G>A	GRCh38
NC_000022.10:g.20127369G>A , CM000684.1:g.20127369G>A	GRCh37
NC_000022.9:g.18507369G>A	NCBI36
NG_021420.1:g.13006G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.511G>A MANE Select	ENSP00000334490.7:p.Val171Met
ENST00000320602.11:c.384+211G>A	ENSP00000317804.7:n.384+211G>A
ENST00000334554.11:c.511G>A	ENSP00000334490.7:p.Val171Met
ENST00000405930.3:c.511G>A	ENSP00000384716.3:p.Val171Met
ENST00000436518.5:c.478G>A	ENSP00000412807.1:p.Val160Met
ENST00000468112.5:n.58-771G>A
NM_001185024.1:c.511G>A	NP_001171953.1:p.Val171Met
NM_013373.3:c.511G>A	NP_037505.1:p.Val171Met
XM_006724239.2:c.511G>A	XP_006724302.1:p.Val171Met
NM_001185024.2:c.511G>A	NP_001171953.1:p.Val171Met
NM_013373.4:c.511G>A MANE Select	NP_037505.1:p.Val171Met