Canonical Allele Identifier: CA2839427245
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47844808dup , CM000674.2:g.47844808dup GRCh38
NC_000012.11:g.48238591dup , CM000674.1:g.48238591dup GRCh37
NC_000012.10:g.46524858dup NCBI36
NG_008731.1:g.65225dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000229022.9:c.1223dup ENSP00000229022.5:p.Glu409Ter
ENST00000549336.6:c.1223dup MANE Select ENSP00000449573.2:p.Glu409Ter
ENST00000229022.7:c.1223dup ENSP00000229022.3:p.Glu409Ter
ENST00000395324.6:c.1223dup ENSP00000378734.2:p.Glu409Ter
ENST00000547065.1:c.*1225dup ENSP00000449074.1:n.*1225dup
ENST00000549336.5:c.1223dup ENSP00000449573.1:p.Glu409Ter
ENST00000550325.5:c.1373dup ENSP00000447173.1:p.Glu459Ter
NM_000376.2:c.1223dup NP_000367.1:p.Glu409Ter
NM_001017535.1:c.1223dup NP_001017535.1:p.Glu409Ter
NM_001017536.1:c.1373dup NP_001017536.1:p.Glu459Ter
XM_006719587.2:c.1223dup XP_006719650.1:p.Glu409Ter
XM_011538720.1:c.1223dup XP_011537022.1:p.Glu409Ter
NM_001364085.1:c.1223dup NP_001351014.1:p.Glu409Ter
XM_006719587.3:c.1223dup XP_006719650.1:p.Glu409Ter
XM_011538720.2:c.1223dup XP_011537022.1:p.Glu409Ter
XM_024449178.1:c.1292dup XP_024304946.1:p.Glu432Ter
NM_000376.3:c.1223dup MANE Select NP_000367.1:p.Glu409Ter
NM_001017535.2:c.1223dup NP_001017535.1:p.Glu409Ter
NM_001017536.2:c.1373dup NP_001017536.1:p.Glu459Ter
NM_001364085.2:c.1223dup NP_001351014.1:p.Glu409Ter
NM_001374661.1:c.1223dup NP_001361590.1:p.Glu409Ter
NM_001374662.1:c.1223dup NP_001361591.1:p.Glu409Ter