Canonical Allele Identifier: CA2370262992

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54154632A= , CM000682.2:g.54154632A=	GRCh38
NC_000020.10:g.52771171A= , CM000682.1:g.52771171A=	GRCh37
NC_000020.9:g.52204578A=	NCBI36
NG_008334.1:g.24346T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000782.5:c.*140T= MANE Select	NP_000773.2:n.*140T=
ENST00000216862.8:c.*140T= MANE Select	ENSP00000216862.3:n.*140T=
NM_000782.4:c.*140T=	NP_000773.2:n.*140T=
NM_001128915.1:c.*140T=	NP_001122387.1:n.*140T=
NM_001128915.2:c.*140T=	NP_001122387.1:n.*140T=
ENST00000216862.7:c.*140T=	ENSP00000216862.3:n.*140T=
ENST00000395955.7:c.*140T=	ENSP00000379285.3:n.*140T=
ENST00000460643.1:n.432T=
XM_005260304.3:c.*312T=	XP_005260361.1:n.*312T=
XM_005260304.5:c.*312T=	XP_005260361.1:n.*312T=
XM_017027691.2:c.*160T=	XP_016883180.1:n.*160T=
XM_017027692.2:c.*10+2537T=	XP_016883181.1:n.*10+2537T=
XM_017027693.2:c.*312T=	XP_016883182.1:n.*312T=