Canonical Allele Identifier: CA2697559200

Gene: VDR

Linked Data

• ClinVar Variation Id: 2714291
• ClinVar RCV Id: RCV003550835

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47845013C>A , CM000674.2:g.47845013C>A	GRCh38
NC_000012.11:g.48238796C>A , CM000674.1:g.48238796C>A	GRCh37
NC_000012.10:g.46525063C>A	NCBI36
NG_008731.1:g.65019G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229022.9:c.1025-8G>T	ENSP00000229022.5:n.1025-8G>T
ENST00000549336.6:c.1025-8G>T MANE Select	ENSP00000449573.2:n.1025-8G>T
ENST00000229022.7:c.1025-8G>T	ENSP00000229022.3:n.1025-8G>T
ENST00000395324.6:c.1025-8G>T	ENSP00000378734.2:n.1025-8G>T
ENST00000547065.1:c.*1027-8G>T	ENSP00000449074.1:n.*1027-8G>T
ENST00000549336.5:c.1025-8G>T	ENSP00000449573.1:n.1025-8G>T
ENST00000550325.5:c.1175-8G>T	ENSP00000447173.1:n.1175-8G>T
NM_000376.2:c.1025-8G>T	NP_000367.1:n.1025-8G>T
NM_001017535.1:c.1025-8G>T	NP_001017535.1:n.1025-8G>T
NM_001017536.1:c.1175-8G>T	NP_001017536.1:n.1175-8G>T
XM_006719587.2:c.1025-8G>T	XP_006719650.1:n.1025-8G>T
XM_011538720.1:c.1025-8G>T	XP_011537022.1:n.1025-8G>T
NM_001364085.1:c.1025-8G>T	NP_001351014.1:n.1025-8G>T
XM_006719587.3:c.1025-8G>T	XP_006719650.1:n.1025-8G>T
XM_011538720.2:c.1025-8G>T	XP_011537022.1:n.1025-8G>T
XM_024449178.1:c.1094-8G>T	XP_024304946.1:n.1094-8G>T
NM_000376.3:c.1025-8G>T MANE Select	NP_000367.1:n.1025-8G>T
NM_001017535.2:c.1025-8G>T	NP_001017535.1:n.1025-8G>T
NM_001017536.2:c.1175-8G>T	NP_001017536.1:n.1175-8G>T
NM_001364085.2:c.1025-8G>T	NP_001351014.1:n.1025-8G>T
NM_001374661.1:c.1025-8G>T	NP_001361590.1:n.1025-8G>T
NM_001374662.1:c.1025-8G>T	NP_001361591.1:n.1025-8G>T