Canonical Allele Identifier: CA638505218

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs1290847410
• gnomAD v2: 22-20127553-G-C
• gnomAD v3: 22-20140030-G-C
• gnomAD v4: 22-20140030-G-C
• MyVariant Identifiers: chr22:g.20127553G>C (hg19) ; chr22:g.20140030G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20140030G>C , CM000684.2:g.20140030G>C	GRCh38
NC_000022.10:g.20127553G>C , CM000684.1:g.20127553G>C	GRCh37
NC_000022.9:g.18507553G>C	NCBI36
NG_021420.1:g.13190G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.558-85G>C MANE Select	ENSP00000334490.7:n.558-85G>C
ENST00000320602.11:c.384+395G>C	ENSP00000317804.7:n.384+395G>C
ENST00000334554.11:c.558-85G>C	ENSP00000334490.7:n.558-85G>C
ENST00000405930.3:c.558-85G>C	ENSP00000384716.3:n.558-85G>C
ENST00000468112.5:n.58-587G>C
ENST00000469212.5:n.94G>C
NM_001185024.1:c.558-85G>C	NP_001171953.1:n.558-85G>C
NM_013373.3:c.558-85G>C	NP_037505.1:n.558-85G>C
XM_006724239.2:c.558-85G>C	XP_006724302.1:n.558-85G>C
NM_001185024.2:c.558-85G>C	NP_001171953.1:n.558-85G>C
NM_013373.4:c.558-85G>C MANE Select	NP_037505.1:n.558-85G>C