Canonical Allele Identifier: CA920236021
Gene: CYP24A1 HGNC NCBI

Linked Data

dbSNP Id: rs1601152889

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173688_54173689del , CM000682.2:g.54173688_54173689del GRCh38
NC_000020.10:g.52790227_52790228del , CM000682.1:g.52790227_52790228del GRCh37
NC_000020.9:g.52223634_52223635del NCBI36
NG_008334.1:g.5290_5291del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-109_-108del MANE Select ENSP00000216862.3:n.-109_-108del
ENST00000216862.7:c.-109_-108del ENSP00000216862.3:n.-109_-108del
NM_000782.4:c.-109_-108del NP_000773.2:n.-109_-108del
NM_001128915.1:c.-109_-108del NP_001122387.1:n.-109_-108del
XM_005260304.3:c.-109_-108del XP_005260361.1:n.-109_-108del
XM_005260304.5:c.-109_-108del XP_005260361.1:n.-109_-108del
XM_017027691.2:c.-109_-108del XP_016883180.1:n.-109_-108del
XM_017027692.2:c.-109_-108del XP_016883181.1:n.-109_-108del
XM_017027693.2:c.-109_-108del XP_016883182.1:n.-109_-108del
NM_000782.5:c.-109_-108del MANE Select NP_000773.2:n.-109_-108del
NM_001128915.2:c.-109_-108del NP_001122387.1:n.-109_-108del