Canonical Allele Identifier: CA638505178

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs1372504998
• gnomAD v2: 22-20127203-C-G
• gnomAD v4: 22-20139680-C-G
• MyVariant Identifiers: chr22:g.20127203C>G (hg19) ; chr22:g.20139680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139680C>G , CM000684.2:g.20139680C>G	GRCh38
NC_000022.10:g.20127203C>G , CM000684.1:g.20127203C>G	GRCh37
NC_000022.9:g.18507203C>G	NCBI36
NG_021420.1:g.12840C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.385-40C>G MANE Select	ENSP00000334490.7:n.385-40C>G
ENST00000320602.11:c.384+45C>G	ENSP00000317804.7:n.384+45C>G
ENST00000334554.11:c.385-40C>G	ENSP00000334490.7:n.385-40C>G
ENST00000405930.3:c.385-40C>G	ENSP00000384716.3:n.385-40C>G
ENST00000436518.5:c.352-40C>G	ENSP00000412807.1:n.352-40C>G
ENST00000468112.5:n.58-937C>G
NM_001185024.1:c.385-40C>G	NP_001171953.1:n.385-40C>G
NM_013373.3:c.385-40C>G	NP_037505.1:n.385-40C>G
XM_006724239.2:c.385-40C>G	XP_006724302.1:n.385-40C>G
NM_001185024.2:c.385-40C>G	NP_001171953.1:n.385-40C>G
NM_013373.4:c.385-40C>G MANE Select	NP_037505.1:n.385-40C>G