Canonical Allele Identifier: CA2370266564

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54162366A= , CM000682.2:g.54162366A=	GRCh38
NC_000020.10:g.52778905A= , CM000682.1:g.52778905A=	GRCh37
NC_000020.9:g.52212312A=	NCBI36
NG_008334.1:g.16612T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216862.8:c.990+351T= MANE Select	ENSP00000216862.3:n.990+351T=
ENST00000216862.7:c.990+351T=	ENSP00000216862.3:n.990+351T=
ENST00000395954.3:c.564+351T=	ENSP00000379284.3:n.564+351T=
ENST00000395955.7:c.990+351T=	ENSP00000379285.3:n.990+351T=
NM_000782.4:c.990+351T=	NP_000773.2:n.990+351T=
NM_001128915.1:c.990+351T=	NP_001122387.1:n.990+351T=
XM_005260304.3:c.990+351T=	XP_005260361.1:n.990+351T=
XM_005260304.5:c.990+351T=	XP_005260361.1:n.990+351T=
XM_017027691.2:c.990+351T=	XP_016883180.1:n.990+351T=
XM_017027692.2:c.990+351T=	XP_016883181.1:n.990+351T=
XM_017027693.2:c.990+351T=	XP_016883182.1:n.990+351T=
NM_000782.5:c.990+351T= MANE Select	NP_000773.2:n.990+351T=
NM_001128915.2:c.990+351T=	NP_001122387.1:n.990+351T=