Canonical Allele Identifier: CA2370263025
Community Standard Title: NM_000782.5(CYP24A1):c.*50C=
Gene: CYP24A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54154722G= , CM000682.2:g.54154722G= GRCh38
NC_000020.10:g.52771261G= , CM000682.1:g.52771261G= GRCh37
NC_000020.9:g.52204668G= NCBI36
NG_008334.1:g.24256C=

Transcript Alleles

HGVS Amino-acid Change
NM_000782.5:c.*50C= MANE Select NP_000773.2:n.*50C=
ENST00000216862.8:c.*50C= MANE Select ENSP00000216862.3:n.*50C=
NM_000782.4:c.*50C= NP_000773.2:n.*50C=
NM_001128915.1:c.*50C= NP_001122387.1:n.*50C=
NM_001128915.2:c.*50C= NP_001122387.1:n.*50C=
ENST00000216862.7:c.*50C= ENSP00000216862.3:n.*50C=
ENST00000395954.3:c.*50C= ENSP00000379284.3:n.*50C=
ENST00000395955.7:c.*50C= ENSP00000379285.3:n.*50C=
ENST00000460643.1:n.342C=
XM_005260304.3:c.*222C= XP_005260361.1:n.*222C=
XM_005260304.5:c.*222C= XP_005260361.1:n.*222C=
XM_017027691.2:c.*70C= XP_016883180.1:n.*70C=
XM_017027692.2:c.*10+2447C= XP_016883181.1:n.*10+2447C=
XM_017027693.2:c.*222C= XP_016883182.1:n.*222C=