Canonical Allele Identifier: CA2655369130

Gene: ZDHHC8

Linked Data

• gnomAD v4: 22-20139835-GCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139836_20139838del , CM000684.2:g.20139836_20139838del	GRCh38
NC_000022.10:g.20127359_20127361del , CM000684.1:g.20127359_20127361del	GRCh37
NC_000022.9:g.18507359_18507361del	NCBI36
NG_021420.1:g.12996_12998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.501_503del MANE Select	ENSP00000334490.7:p.Leu168del
ENST00000320602.11:c.384+201_384+203del	ENSP00000317804.7:n.384+201_384+203del
ENST00000334554.11:c.501_503del	ENSP00000334490.7:p.Leu168del
ENST00000405930.3:c.501_503del	ENSP00000384716.3:p.Leu168del
ENST00000436518.5:c.468_470del	ENSP00000412807.1:p.Leu157del
ENST00000468112.5:n.58-781_58-779del
NM_001185024.1:c.501_503del	NP_001171953.1:p.Leu168del
NM_013373.3:c.501_503del	NP_037505.1:p.Leu168del
XM_006724239.2:c.501_503del	XP_006724302.1:p.Leu168del
NM_001185024.2:c.501_503del	NP_001171953.1:p.Leu168del
NM_013373.4:c.501_503del MANE Select	NP_037505.1:p.Leu168del