Canonical Allele Identifier: CA410734256
Gene: ZDHHC8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139790T>C , CM000684.2:g.20139790T>C GRCh38
NC_000022.10:g.20127313T>C , CM000684.1:g.20127313T>C GRCh37
NC_000022.9:g.18507313T>C NCBI36
NG_021420.1:g.12950T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.455T>C MANE Select ENSP00000334490.7:p.Phe152Ser
ENST00000320602.11:c.384+155T>C ENSP00000317804.7:n.384+155T>C
ENST00000334554.11:c.455T>C ENSP00000334490.7:p.Phe152Ser
ENST00000405930.3:c.455T>C ENSP00000384716.3:p.Phe152Ser
ENST00000436518.5:c.422T>C ENSP00000412807.1:p.Phe141Ser
ENST00000468112.5:n.58-827T>C
NM_001185024.1:c.455T>C NP_001171953.1:p.Phe152Ser
NM_013373.3:c.455T>C NP_037505.1:p.Phe152Ser
XM_006724239.2:c.455T>C XP_006724302.1:p.Phe152Ser
NM_001185024.2:c.455T>C NP_001171953.1:p.Phe152Ser
NM_013373.4:c.455T>C MANE Select NP_037505.1:p.Phe152Ser