Canonical Allele Identifier: CA2370264628

Gene: CYP24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54158096A= , CM000682.2:g.54158096A=	GRCh38
NC_000020.10:g.52774635A= , CM000682.1:g.52774635A=	GRCh37
NC_000020.9:g.52208042A=	NCBI36
NG_008334.1:g.20882T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000782.5:c.1226T= MANE Select	NP_000773.2:p.Leu409=
ENST00000216862.8:c.1226T= MANE Select	ENSP00000216862.3:p.Leu409=
NM_000782.4:c.1226T=	NP_000773.2:p.Leu409=
NM_001128915.1:c.1226T=	NP_001122387.1:p.Leu409=
NM_001128915.2:c.1226T=	NP_001122387.1:p.Leu409=
ENST00000216862.7:c.1226T=	ENSP00000216862.3:p.Leu409=
ENST00000395954.3:c.800T=	ENSP00000379284.3:p.Leu267=
ENST00000395955.7:c.1226T=	ENSP00000379285.3:p.Leu409=
XM_005260304.3:c.1226T=	XP_005260361.1:p.Leu409=
XM_005260304.5:c.1226T=	XP_005260361.1:p.Leu409=
XM_017027691.2:c.1226T=	XP_016883180.1:p.Leu409=
XM_017027692.2:c.1226T=	XP_016883181.1:p.Leu409=
XM_017027693.2:c.1226T=	XP_016883182.1:p.Leu409=