Canonical Allele Identifier: CA2396214297
Gene: ZDHHC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139909T= , CM000684.2:g.20139909T= GRCh38
NC_000022.10:g.20127432T= , CM000684.1:g.20127432T= GRCh37
NC_000022.9:g.18507432T= NCBI36
NG_021420.1:g.13069T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.557+17T= MANE Select ENSP00000334490.7:n.557+17T=
ENST00000320602.11:c.384+274T= ENSP00000317804.7:n.384+274T=
ENST00000334554.11:c.557+17T= ENSP00000334490.7:n.557+17T=
ENST00000405930.3:c.557+17T= ENSP00000384716.3:n.557+17T=
ENST00000436518.5:c.541T=
ENST00000468112.5:n.58-708T=
NM_001185024.1:c.557+17T= NP_001171953.1:n.557+17T=
NM_013373.3:c.557+17T= NP_037505.1:n.557+17T=
XM_006724239.2:c.557+17T= XP_006724302.1:n.557+17T=
NM_001185024.2:c.557+17T= NP_001171953.1:n.557+17T=
NM_013373.4:c.557+17T= MANE Select NP_037505.1:n.557+17T=