Canonical Allele Identifier: CA10108534
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs368880536

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139539G>A , CM000684.2:g.20139539G>A GRCh38
NC_000022.10:g.20127062G>A , CM000684.1:g.20127062G>A GRCh37
NC_000022.9:g.18507062G>A NCBI36
NG_021420.1:g.12699G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.288G>A MANE Select ENSP00000334490.7:p.Val96=
ENST00000320602.11:c.288G>A ENSP00000317804.7:p.Val96=
ENST00000334554.11:c.288G>A ENSP00000334490.7:p.Val96=
ENST00000405930.3:c.288G>A ENSP00000384716.3:p.Val96=
ENST00000436518.5:c.255G>A ENSP00000412807.1:p.Val85=
ENST00000468112.5:n.58-1078G>A
NM_001185024.1:c.288G>A NP_001171953.1:p.Val96=
NM_013373.3:c.288G>A NP_037505.1:p.Val96=
XM_006724239.2:c.288G>A XP_006724302.1:p.Val96=
NM_001185024.2:c.288G>A NP_001171953.1:p.Val96=
NM_013373.4:c.288G>A MANE Select NP_037505.1:p.Val96=