Canonical Allele Identifier: CA6533707
Gene: VDR HGNC NCBI

Linked Data

dbSNP Id: rs368685381

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47844729G>A , CM000674.2:g.47844729G>A GRCh38
NC_000012.11:g.48238512G>A , CM000674.1:g.48238512G>A GRCh37
NC_000012.10:g.46524779G>A NCBI36
NG_008731.1:g.65303C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229022.9:c.1301C>T ENSP00000229022.5:p.Ala434Val
ENST00000549336.6:c.*17C>T MANE Select ENSP00000449573.2:n.*17C>T
ENST00000229022.7:c.*17C>T ENSP00000229022.3:n.*17C>T
ENST00000395324.6:c.*17C>T ENSP00000378734.2:n.*17C>T
ENST00000547065.1:c.*1303C>T ENSP00000449074.1:n.*1303C>T
ENST00000549336.5:c.*17C>T ENSP00000449573.1:n.*17C>T
ENST00000550325.5:c.*17C>T ENSP00000447173.1:n.*17C>T
NM_000376.2:c.*17C>T NP_000367.1:n.*17C>T
NM_001017535.1:c.*17C>T NP_001017535.1:n.*17C>T
NM_001017536.1:c.*17C>T NP_001017536.1:n.*17C>T
XM_006719587.2:c.*17C>T XP_006719650.1:n.*17C>T
XM_011538720.1:c.*17C>T XP_011537022.1:n.*17C>T
NM_001364085.1:c.1301C>T NP_001351014.1:p.Ala434Val
NM_000376.3:c.*17C>T MANE Select NP_000367.1:n.*17C>T
NM_001017535.2:c.*17C>T NP_001017535.1:n.*17C>T
NM_001017536.2:c.*17C>T NP_001017536.1:n.*17C>T
NM_001364085.2:c.1301C>T NP_001351014.1:p.Ala434Val
NM_001374661.1:c.*17C>T NP_001361590.1:n.*17C>T
NM_001374662.1:c.*17C>T NP_001361591.1:n.*17C>T