Canonical Allele Identifier: CA2396214202
Gene: ZDHHC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139657G= , CM000684.2:g.20139657G= GRCh38
NC_000022.10:g.20127180G= , CM000684.1:g.20127180G= GRCh37
NC_000022.9:g.18507180G= NCBI36
NG_021420.1:g.12817G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.384+22G= MANE Select ENSP00000334490.7:n.384+22G=
ENST00000320602.11:c.384+22G= ENSP00000317804.7:n.384+22G=
ENST00000334554.11:c.384+22G= ENSP00000334490.7:n.384+22G=
ENST00000405930.3:c.384+22G= ENSP00000384716.3:n.384+22G=
ENST00000436518.5:c.351+22G= ENSP00000412807.1:n.351+22G=
ENST00000468112.5:n.58-960G=
NM_001185024.1:c.384+22G= NP_001171953.1:n.384+22G=
NM_013373.3:c.384+22G= NP_037505.1:n.384+22G=
XM_006724239.2:c.384+22G= XP_006724302.1:n.384+22G=
NM_001185024.2:c.384+22G= NP_001171953.1:n.384+22G=
NM_013373.4:c.384+22G= MANE Select NP_037505.1:n.384+22G=