Canonical Allele Identifier: CA10108541

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs773406474
• ExAC: 22:20127103 A / G
• gnomAD v2: 22-20127103-A-G
• gnomAD v4: 22-20139580-A-G
• MyVariant Identifiers: chr22:g.20127103A>G (hg19) ; chr22:g.20139580A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139580A>G , CM000684.2:g.20139580A>G	GRCh38
NC_000022.10:g.20127103A>G , CM000684.1:g.20127103A>G	GRCh37
NC_000022.9:g.18507103A>G	NCBI36
NG_021420.1:g.12740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.329A>G MANE Select	ENSP00000334490.7:p.His110Arg
ENST00000320602.11:c.329A>G	ENSP00000317804.7:p.His110Arg
ENST00000334554.11:c.329A>G	ENSP00000334490.7:p.His110Arg
ENST00000405930.3:c.329A>G	ENSP00000384716.3:p.His110Arg
ENST00000436518.5:c.296A>G	ENSP00000412807.1:p.His99Arg
ENST00000468112.5:n.58-1037A>G
NM_001185024.1:c.329A>G	NP_001171953.1:p.His110Arg
NM_013373.3:c.329A>G	NP_037505.1:p.His110Arg
XM_006724239.2:c.329A>G	XP_006724302.1:p.His110Arg
NM_001185024.2:c.329A>G	NP_001171953.1:p.His110Arg
NM_013373.4:c.329A>G MANE Select	NP_037505.1:p.His110Arg