Canonical Allele Identifier: CA2370272019

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54173679A= , CM000682.2:g.54173679A=	GRCh38
NC_000020.10:g.52790218A= , CM000682.1:g.52790218A=	GRCh37
NC_000020.9:g.52223625A=	NCBI36
NG_008334.1:g.5299T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.-100T= MANE Select	ENSP00000216862.3:n.-100T=
ENST00000216862.7:c.-100T=	ENSP00000216862.3:n.-100T=
NM_000782.4:c.-100T=	NP_000773.2:n.-100T=
NM_001128915.1:c.-100T=	NP_001122387.1:n.-100T=
XM_005260304.3:c.-100T=	XP_005260361.1:n.-100T=
XM_005260304.5:c.-100T=	XP_005260361.1:n.-100T=
XM_017027691.2:c.-100T=	XP_016883180.1:n.-100T=
XM_017027692.2:c.-100T=	XP_016883181.1:n.-100T=
XM_017027693.2:c.-100T=	XP_016883182.1:n.-100T=
NM_000782.5:c.-100T= MANE Select	NP_000773.2:n.-100T=
NM_001128915.2:c.-100T=	NP_001122387.1:n.-100T=