Canonical Allele Identifier: CA2618496886
Gene: VDR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47844699G>T , CM000674.2:g.47844699G>T GRCh38
NC_000012.11:g.48238482G>T , CM000674.1:g.48238482G>T GRCh37
NC_000012.10:g.46524749G>T NCBI36
NG_008731.1:g.65333C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229022.9:c.1331C>A ENSP00000229022.5:p.Ala444Asp
ENST00000549336.6:c.*47C>A MANE Select ENSP00000449573.2:n.*47C>A
ENST00000229022.7:c.*47C>A ENSP00000229022.3:n.*47C>A
ENST00000395324.6:c.*47C>A ENSP00000378734.2:n.*47C>A
ENST00000547065.1:c.*1333C>A ENSP00000449074.1:n.*1333C>A
ENST00000549336.5:c.*47C>A ENSP00000449573.1:n.*47C>A
ENST00000550325.5:c.*47C>A ENSP00000447173.1:n.*47C>A
NM_000376.2:c.*47C>A NP_000367.1:n.*47C>A
NM_001017535.1:c.*47C>A NP_001017535.1:n.*47C>A
NM_001017536.1:c.*47C>A NP_001017536.1:n.*47C>A
XM_006719587.2:c.*47C>A XP_006719650.1:n.*47C>A
XM_011538720.1:c.*47C>A XP_011537022.1:n.*47C>A
NM_001364085.1:c.1331C>A NP_001351014.1:p.Ala444Asp
NM_000376.3:c.*47C>A MANE Select NP_000367.1:n.*47C>A
NM_001017535.2:c.*47C>A NP_001017535.1:n.*47C>A
NM_001017536.2:c.*47C>A NP_001017536.1:n.*47C>A
NM_001364085.2:c.1331C>A NP_001351014.1:p.Ala444Asp
NM_001374661.1:c.*47C>A NP_001361590.1:n.*47C>A
NM_001374662.1:c.*47C>A NP_001361591.1:n.*47C>A