Canonical Allele Identifier: CA10108524

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs773638097
• ExAC: 22:20127019 A / T
• gnomAD v2: 22-20127019-A-T
• gnomAD v4: 22-20139496-A-T
• MyVariant Identifiers: chr22:g.20127019A>T (hg19) ; chr22:g.20139496A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139496A>T , CM000684.2:g.20139496A>T	GRCh38
NC_000022.10:g.20127019A>T , CM000684.1:g.20127019A>T	GRCh37
NC_000022.9:g.18507019A>T	NCBI36
NG_021420.1:g.12656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.245A>T MANE Select	ENSP00000334490.7:p.Lys82Met
ENST00000320602.11:c.245A>T	ENSP00000317804.7:p.Lys82Met
ENST00000334554.11:c.245A>T	ENSP00000334490.7:p.Lys82Met
ENST00000405930.3:c.245A>T	ENSP00000384716.3:p.Lys82Met
ENST00000436518.5:c.212A>T	ENSP00000412807.1:p.Lys71Met
ENST00000468112.5:n.58-1121A>T
NM_001185024.1:c.245A>T	NP_001171953.1:p.Lys82Met
NM_013373.3:c.245A>T	NP_037505.1:p.Lys82Met
XM_006724239.2:c.245A>T	XP_006724302.1:p.Lys82Met
NM_001185024.2:c.245A>T	NP_001171953.1:p.Lys82Met
NM_013373.4:c.245A>T MANE Select	NP_037505.1:p.Lys82Met