Canonical Allele Identifier: CA2370267411

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54164299T= , CM000682.2:g.54164299T=	GRCh38
NC_000020.10:g.52780838T= , CM000682.1:g.52780838T=	GRCh37
NC_000020.9:g.52214245T=	NCBI36
NG_008334.1:g.14679A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216862.8:c.844+153A= MANE Select	ENSP00000216862.3:n.844+153A=
ENST00000216862.7:c.844+153A=	ENSP00000216862.3:n.844+153A=
ENST00000395954.3:c.418+153A=	ENSP00000379284.3:n.418+153A=
ENST00000395955.7:c.844+153A=	ENSP00000379285.3:n.844+153A=
ENST00000487593.1:n.97+153A=
NM_000782.4:c.844+153A=	NP_000773.2:n.844+153A=
NM_001128915.1:c.844+153A=	NP_001122387.1:n.844+153A=
XM_005260304.3:c.844+153A=	XP_005260361.1:n.844+153A=
XM_005260304.5:c.844+153A=	XP_005260361.1:n.844+153A=
XM_017027691.2:c.844+153A=	XP_016883180.1:n.844+153A=
XM_017027692.2:c.844+153A=	XP_016883181.1:n.844+153A=
XM_017027693.2:c.844+153A=	XP_016883182.1:n.844+153A=
NM_000782.5:c.844+153A= MANE Select	NP_000773.2:n.844+153A=
NM_001128915.2:c.844+153A=	NP_001122387.1:n.844+153A=