Canonical Allele Identifier: CA605231303

Gene: VDR

Linked Data

• dbSNP Id: rs1324371157
• gnomAD v2: 12-48238486-T-A
• gnomAD v3: 12-47844703-T-A
• gnomAD v4: 12-47844703-T-A
• MyVariant Identifiers: chr12:g.48238486T>A (hg19) ; chr12:g.47844703T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47844703T>A , CM000674.2:g.47844703T>A	GRCh38
NC_000012.11:g.48238486T>A , CM000674.1:g.48238486T>A	GRCh37
NC_000012.10:g.46524753T>A	NCBI36
NG_008731.1:g.65329A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.1327A>T	ENSP00000229022.5:p.Arg443Trp
ENST00000549336.6:c.*43A>T MANE Select	ENSP00000449573.2:n.*43A>T
ENST00000229022.7:c.*43A>T	ENSP00000229022.3:n.*43A>T
ENST00000395324.6:c.*43A>T	ENSP00000378734.2:n.*43A>T
ENST00000547065.1:c.*1329A>T	ENSP00000449074.1:n.*1329A>T
ENST00000549336.5:c.*43A>T	ENSP00000449573.1:n.*43A>T
ENST00000550325.5:c.*43A>T	ENSP00000447173.1:n.*43A>T
NM_000376.2:c.*43A>T	NP_000367.1:n.*43A>T
NM_001017535.1:c.*43A>T	NP_001017535.1:n.*43A>T
NM_001017536.1:c.*43A>T	NP_001017536.1:n.*43A>T
XM_006719587.2:c.*43A>T	XP_006719650.1:n.*43A>T
XM_011538720.1:c.*43A>T	XP_011537022.1:n.*43A>T
NM_001364085.1:c.1327A>T	NP_001351014.1:p.Arg443Trp
NM_000376.3:c.*43A>T MANE Select	NP_000367.1:n.*43A>T
NM_001017535.2:c.*43A>T	NP_001017535.1:n.*43A>T
NM_001017536.2:c.*43A>T	NP_001017536.1:n.*43A>T
NM_001364085.2:c.1327A>T	NP_001351014.1:p.Arg443Trp
NM_001374661.1:c.*43A>T	NP_001361590.1:n.*43A>T
NM_001374662.1:c.*43A>T	NP_001361591.1:n.*43A>T