Canonical Allele Identifier: CA10108528
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs151053498
ExAC: 22:20127034 G / A
gnomAD v2: 22-20127034-G-A
gnomAD v3: 22-20139511-G-A
gnomAD v4: 22-20139511-G-A
COSMIC: COSM1616242 COSM1616243
MyVariant Identifiers: chr22:g.20127034G>A (hg19) chr22:g.20139511G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139511G>A , CM000684.2:g.20139511G>A GRCh38
NC_000022.10:g.20127034G>A , CM000684.1:g.20127034G>A GRCh37
NC_000022.9:g.18507034G>A NCBI36
NG_021420.1:g.12671G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.260G>A MANE Select ENSP00000334490.7:p.Arg87Gln
ENST00000320602.11:c.260G>A ENSP00000317804.7:p.Arg87Gln
ENST00000334554.11:c.260G>A ENSP00000334490.7:p.Arg87Gln
ENST00000405930.3:c.260G>A ENSP00000384716.3:p.Arg87Gln
ENST00000436518.5:c.227G>A ENSP00000412807.1:p.Arg76Gln
ENST00000468112.5:n.58-1106G>A
NM_001185024.1:c.260G>A NP_001171953.1:p.Arg87Gln
NM_013373.3:c.260G>A NP_037505.1:p.Arg87Gln
XM_006724239.2:c.260G>A XP_006724302.1:p.Arg87Gln
NM_001185024.2:c.260G>A NP_001171953.1:p.Arg87Gln
NM_013373.4:c.260G>A MANE Select NP_037505.1:p.Arg87Gln
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