Canonical Allele Identifier: CA2034408807

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47844527C= , CM000674.2:g.47844527C=	GRCh38
NC_000012.11:g.48238310C= , CM000674.1:g.48238310C=	GRCh37
NC_000012.10:g.46524577C=	NCBI36
NG_008731.1:g.65505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.*18G=	ENSP00000229022.5:n.*18G=
ENST00000549336.6:c.*219G= MANE Select	ENSP00000449573.2:n.*219G=
ENST00000229022.7:c.*219G=	ENSP00000229022.3:n.*219G=
ENST00000395324.6:c.*219G=	ENSP00000378734.2:n.*219G=
ENST00000547065.1:c.*1505G=	ENSP00000449074.1:n.*1505G=
ENST00000549336.5:c.*219G=	ENSP00000449573.1:n.*219G=
ENST00000550325.5:c.*219G=	ENSP00000447173.1:n.*219G=
NM_000376.2:c.*219G=	NP_000367.1:n.*219G=
NM_001017535.1:c.*219G=	NP_001017535.1:n.*219G=
NM_001017536.1:c.*219G=	NP_001017536.1:n.*219G=
XM_006719587.2:c.*219G=	XP_006719650.1:n.*219G=
XM_011538720.1:c.*219G=	XP_011537022.1:n.*219G=
NM_001364085.1:c.*18G=	NP_001351014.1:n.*18G=
NM_000376.3:c.*219G= MANE Select	NP_000367.1:n.*219G=
NM_001017535.2:c.*219G=	NP_001017535.1:n.*219G=
NM_001017536.2:c.*219G=	NP_001017536.1:n.*219G=
NM_001364085.2:c.*18G=	NP_001351014.1:n.*18G=
NM_001374661.1:c.*219G=	NP_001361590.1:n.*219G=
NM_001374662.1:c.*219G=	NP_001361591.1:n.*219G=