Canonical Allele Identifier: CA645372517
Gene: ZDHHC24 HGNC NCBI

Linked Data

ClinVar Variation Id: 431737
ClinVar RCV Id: RCV000497465

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66528892_66536798del , CM000673.2:g.66528892_66536798del GRCh38
NC_000011.9:g.66296363_66304269del , CM000673.1:g.66296363_66304269del GRCh37
NC_000011.8:g.66052939_66060845del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000526986.5:c.559+6908_736+422del
ENST00000534073.5:c.559+6908_560-1884del ENSP00000436503.1:n.559+6908_560-1884del
XM_005273874.3:c.559+6908_560-1884del XP_005273931.1:n.559+6908_560-1884del
XM_011544894.1:c.559+6908_560-1884del XP_011543196.1:n.559+6908_560-1884del
XM_011544895.1:c.559+6908_560-4614del XP_011543197.1:n.559+6908_560-4614del
XR_949860.1:n.615+6908_616-1884del
NM_001348571.1:c.559+6908_736+422del
XM_005273874.4:c.559+6908_560-1884del XP_005273931.1:n.559+6908_560-1884del
XM_011544894.2:c.559+6908_560-1884del XP_011543196.1:n.559+6908_560-1884del
XR_001747823.2:n.740+6908_741-4614del
XR_949860.3:n.740+6908_741-1884del
NM_001348571.2:c.559+6908_736+422del