Canonical Allele Identifier: CA2655369495
Gene: ZDHHC8 HGNC NCBI

Linked Data

gnomAD v4: 22-20139991-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139991G>C , CM000684.2:g.20139991G>C GRCh38
NC_000022.10:g.20127514G>C , CM000684.1:g.20127514G>C GRCh37
NC_000022.9:g.18507514G>C NCBI36
NG_021420.1:g.13151G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.557+99G>C MANE Select ENSP00000334490.7:n.557+99G>C
ENST00000320602.11:c.384+356G>C ENSP00000317804.7:n.384+356G>C
ENST00000334554.11:c.557+99G>C ENSP00000334490.7:n.557+99G>C
ENST00000405930.3:c.557+99G>C ENSP00000384716.3:n.557+99G>C
ENST00000468112.5:n.58-626G>C
ENST00000469212.5:n.55G>C
NM_001185024.1:c.557+99G>C NP_001171953.1:n.557+99G>C
NM_013373.3:c.557+99G>C NP_037505.1:n.557+99G>C
XM_006724239.2:c.557+99G>C XP_006724302.1:n.557+99G>C
NM_001185024.2:c.557+99G>C NP_001171953.1:n.557+99G>C
NM_013373.4:c.557+99G>C MANE Select NP_037505.1:n.557+99G>C
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