Canonical Allele Identifier: CA2370272082

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54173791T= , CM000682.2:g.54173791T=	GRCh38
NC_000020.10:g.52790330T= , CM000682.1:g.52790330T=	GRCh37
NC_000020.9:g.52223737T=	NCBI36
NG_008334.1:g.5187A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.-212A= MANE Select	ENSP00000216862.3:n.-212A=
ENST00000216862.7:c.-212A=	ENSP00000216862.3:n.-212A=
NM_000782.4:c.-212A=	NP_000773.2:n.-212A=
NM_001128915.1:c.-212A=	NP_001122387.1:n.-212A=
XM_005260304.3:c.-212A=	XP_005260361.1:n.-212A=
XM_005260304.5:c.-212A=	XP_005260361.1:n.-212A=
XM_017027691.2:c.-212A=	XP_016883180.1:n.-212A=
XM_017027692.2:c.-212A=	XP_016883181.1:n.-212A=
XM_017027693.2:c.-212A=	XP_016883182.1:n.-212A=
NM_000782.5:c.-212A= MANE Select	NP_000773.2:n.-212A=
NM_001128915.2:c.-212A=	NP_001122387.1:n.-212A=