Canonical Allele Identifier: CA2370272048
Gene: CYP24A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173732C= , CM000682.2:g.54173732C= GRCh38
NC_000020.10:g.52790271C= , CM000682.1:g.52790271C= GRCh37
NC_000020.9:g.52223678C= NCBI36
NG_008334.1:g.5246G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-153G= MANE Select ENSP00000216862.3:n.-153G=
ENST00000216862.7:c.-153G= ENSP00000216862.3:n.-153G=
NM_000782.4:c.-153G= NP_000773.2:n.-153G=
NM_001128915.1:c.-153G= NP_001122387.1:n.-153G=
XM_005260304.3:c.-153G= XP_005260361.1:n.-153G=
XM_005260304.5:c.-153G= XP_005260361.1:n.-153G=
XM_017027691.2:c.-153G= XP_016883180.1:n.-153G=
XM_017027692.2:c.-153G= XP_016883181.1:n.-153G=
XM_017027693.2:c.-153G= XP_016883182.1:n.-153G=
NM_000782.5:c.-153G= MANE Select NP_000773.2:n.-153G=
NM_001128915.2:c.-153G= NP_001122387.1:n.-153G=