Canonical Allele Identifier: CA2653396749
Gene: CYP24A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54164313del , CM000682.2:g.54164313del GRCh38
NC_000020.10:g.52780852del , CM000682.1:g.52780852del GRCh37
NC_000020.9:g.52214259del NCBI36
NG_008334.1:g.14668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.844+142del MANE Select ENSP00000216862.3:n.844+142del
ENST00000216862.7:c.844+142del ENSP00000216862.3:n.844+142del
ENST00000395954.3:c.418+142del ENSP00000379284.3:n.418+142del
ENST00000395955.7:c.844+142del ENSP00000379285.3:n.844+142del
ENST00000487593.1:n.97+142del
NM_000782.4:c.844+142del NP_000773.2:n.844+142del
NM_001128915.1:c.844+142del NP_001122387.1:n.844+142del
XM_005260304.3:c.844+142del XP_005260361.1:n.844+142del
XM_005260304.5:c.844+142del XP_005260361.1:n.844+142del
XM_017027691.2:c.844+142del XP_016883180.1:n.844+142del
XM_017027692.2:c.844+142del XP_016883181.1:n.844+142del
XM_017027693.2:c.844+142del XP_016883182.1:n.844+142del
NM_000782.5:c.844+142del MANE Select NP_000773.2:n.844+142del
NM_001128915.2:c.844+142del NP_001122387.1:n.844+142del