Canonical Allele Identifier: CA2655369481
Gene: ZDHHC8 HGNC NCBI

Linked Data

gnomAD v4: 22-20139967-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139967T>A , CM000684.2:g.20139967T>A GRCh38
NC_000022.10:g.20127490T>A , CM000684.1:g.20127490T>A GRCh37
NC_000022.9:g.18507490T>A NCBI36
NG_021420.1:g.13127T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334554.12:c.557+75T>A MANE Select ENSP00000334490.7:n.557+75T>A
ENST00000320602.11:c.384+332T>A ENSP00000317804.7:n.384+332T>A
ENST00000334554.11:c.557+75T>A ENSP00000334490.7:n.557+75T>A
ENST00000405930.3:c.557+75T>A ENSP00000384716.3:n.557+75T>A
ENST00000468112.5:n.58-650T>A
ENST00000469212.5:n.31T>A
NM_001185024.1:c.557+75T>A NP_001171953.1:n.557+75T>A
NM_013373.3:c.557+75T>A NP_037505.1:n.557+75T>A
XM_006724239.2:c.557+75T>A XP_006724302.1:n.557+75T>A
NM_001185024.2:c.557+75T>A NP_001171953.1:n.557+75T>A
NM_013373.4:c.557+75T>A MANE Select NP_037505.1:n.557+75T>A
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