Canonical Allele Identifier: CA2370267503
Gene: CYP24A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54164501G= , CM000682.2:g.54164501G= GRCh38
NC_000020.10:g.52781040G= , CM000682.1:g.52781040G= GRCh37
NC_000020.9:g.52214447G= NCBI36
NG_008334.1:g.14477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.795C= MANE Select ENSP00000216862.3:p.Thr265=
ENST00000216862.7:c.795C= ENSP00000216862.3:p.Thr265=
ENST00000395954.3:c.369C= ENSP00000379284.3:p.Thr123=
ENST00000395955.7:c.795C= ENSP00000379285.3:p.Thr265=
ENST00000487593.1:n.48C=
NM_000782.4:c.795C= NP_000773.2:p.Thr265=
NM_001128915.1:c.795C= NP_001122387.1:p.Thr265=
XM_005260304.3:c.795C= XP_005260361.1:p.Thr265=
XM_005260304.5:c.795C= XP_005260361.1:p.Thr265=
XM_017027691.2:c.795C= XP_016883180.1:p.Thr265=
XM_017027692.2:c.795C= XP_016883181.1:p.Thr265=
XM_017027693.2:c.795C= XP_016883182.1:p.Thr265=
NM_000782.5:c.795C= MANE Select NP_000773.2:p.Thr265=
NM_001128915.2:c.795C= NP_001122387.1:p.Thr265=