Canonical Allele Identifier: CA1024164210
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs2050454345

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20140053T>A , CM000684.2:g.20140053T>A GRCh38
NC_000022.10:g.20127576T>A , CM000684.1:g.20127576T>A GRCh37
NC_000022.9:g.18507576T>A NCBI36
NG_021420.1:g.13213T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334554.12:c.558-62T>A MANE Select ENSP00000334490.7:n.558-62T>A
ENST00000320602.11:c.384+418T>A ENSP00000317804.7:n.384+418T>A
ENST00000334554.11:c.558-62T>A ENSP00000334490.7:n.558-62T>A
ENST00000405930.3:c.558-62T>A ENSP00000384716.3:n.558-62T>A
ENST00000468112.5:n.58-564T>A
ENST00000469212.5:n.117T>A
NM_001185024.1:c.558-62T>A NP_001171953.1:n.558-62T>A
NM_013373.3:c.558-62T>A NP_037505.1:n.558-62T>A
XM_006724239.2:c.558-62T>A XP_006724302.1:n.558-62T>A
NM_001185024.2:c.558-62T>A NP_001171953.1:n.558-62T>A
NM_013373.4:c.558-62T>A MANE Select NP_037505.1:n.558-62T>A