Canonical Allele Identifier: CA2034409818

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47846674A= , CM000674.2:g.47846674A=	GRCh38
NC_000012.11:g.48240457A= , CM000674.1:g.48240457A=	GRCh37
NC_000012.10:g.46526724A=	NCBI36
NG_008731.1:g.63358T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.890T=	ENSP00000229022.5:p.Val297=
ENST00000549336.6:c.890T= MANE Select	ENSP00000449573.2:p.Val297=
ENST00000229022.7:c.890T=	ENSP00000229022.3:p.Val297=
ENST00000395324.6:c.890T=	ENSP00000378734.2:p.Val297=
ENST00000547065.1:c.*892T=	ENSP00000449074.1:n.*892T=
ENST00000549336.5:c.890T=	ENSP00000449573.1:p.Val297=
ENST00000550325.5:c.1040T=	ENSP00000447173.1:p.Val347=
NM_000376.2:c.890T=	NP_000367.1:p.Val297=
NM_001017535.1:c.890T=	NP_001017535.1:p.Val297=
NM_001017536.1:c.1040T=	NP_001017536.1:p.Val347=
XM_006719587.2:c.890T=	XP_006719650.1:p.Val297=
XM_011538720.1:c.890T=	XP_011537022.1:p.Val297=
NM_001364085.1:c.890T=	NP_001351014.1:p.Val297=
XM_006719587.3:c.890T=	XP_006719650.1:p.Val297=
XM_011538720.2:c.890T=	XP_011537022.1:p.Val297=
XM_024449178.1:c.959T=	XP_024304946.1:p.Val320=
NM_000376.3:c.890T= MANE Select	NP_000367.1:p.Val297=
NM_001017535.2:c.890T=	NP_001017535.1:p.Val297=
NM_001017536.2:c.1040T=	NP_001017536.1:p.Val347=
NM_001364085.2:c.890T=	NP_001351014.1:p.Val297=
NM_001374661.1:c.890T=	NP_001361590.1:p.Val297=
NM_001374662.1:c.890T=	NP_001361591.1:p.Val297=