Canonical Allele Identifier: CA12360005
Gene: ZDHHC14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157620251G>A , CM000668.2:g.157620251G>A GRCh38
NC_000006.11:g.158041283G>A , CM000668.1:g.158041283G>A GRCh37
NC_000006.10:g.157961271G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359775.10:c.566-8098G>A MANE Select ENSP00000352821.5:n.566-8098G>A
ENST00000340347.7:c.139-8197G>A
ENST00000341375.12:n.217-8098G>A
ENST00000359775.9:c.566-8098G>A ENSP00000352821.5:n.566-8098G>A
ENST00000414563.6:c.566-8098G>A ENSP00000410713.2:n.566-8098G>A
ENST00000518214.5:c.321-8098G>A
ENST00000523468.5:n.317-8098G>A
NM_024630.2:c.566-8098G>A NP_078906.2:n.566-8098G>A
NM_153746.1:c.566-8098G>A NP_714968.1:n.566-8098G>A
XM_005267146.2:c.-68-8098G>A XP_005267203.1:n.-68-8098G>A
XM_011536119.1:c.566-8098G>A XP_011534421.1:n.566-8098G>A
XM_011536120.1:c.440-8098G>A XP_011534422.1:n.440-8098G>A
XM_011536121.1:c.566-8098G>A XP_011534423.1:n.566-8098G>A
XM_011536122.1:c.566-12583G>A XP_011534424.1:n.566-12583G>A
XM_011536123.1:c.251-8098G>A XP_011534425.1:n.251-8098G>A
XM_011536124.1:c.566-8098G>A XP_011534426.1:n.566-8098G>A
XM_005267146.3:c.-68-8098G>A XP_005267203.1:n.-68-8098G>A
XM_011536120.2:c.440-8098G>A XP_011534422.1:n.440-8098G>A
XM_011536123.2:c.251-8098G>A XP_011534425.1:n.251-8098G>A
XM_017011307.1:c.620-8098G>A XP_016866796.1:n.620-8098G>A
XM_017011308.1:c.620-8098G>A XP_016866797.1:n.620-8098G>A
XM_017011309.1:c.620-8098G>A XP_016866798.1:n.620-8098G>A
XM_017011310.1:c.620-8098G>A XP_016866799.1:n.620-8098G>A
XM_017011311.1:c.620-12583G>A XP_016866800.1:n.620-12583G>A
XM_017011312.1:c.251-8098G>A XP_016866801.1:n.251-8098G>A
NM_024630.3:c.566-8098G>A MANE Select NP_078906.2:n.566-8098G>A
NM_153746.2:c.566-8098G>A NP_714968.1:n.566-8098G>A
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