Canonical Allele Identifier: CA2795862184
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47845083_47845084insAAA , CM000674.2:g.47845083_47845084insAAA GRCh38
NC_000012.11:g.48238866_48238867insAAA , CM000674.1:g.48238866_48238867insAAA GRCh37
NC_000012.10:g.46525133_46525134insAAA NCBI36
NG_008731.1:g.64948_64949insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000229022.9:c.1025-79_1025-78insTTT ENSP00000229022.5:n.1025-79_1025-78insTTT
ENST00000549336.6:c.1025-79_1025-78insTTT MANE Select ENSP00000449573.2:n.1025-79_1025-78insTTT
ENST00000229022.7:c.1025-79_1025-78insTTT ENSP00000229022.3:n.1025-79_1025-78insTTT
ENST00000395324.6:c.1025-79_1025-78insTTT ENSP00000378734.2:n.1025-79_1025-78insTTT
ENST00000547065.1:c.*1027-79_*1027-78insTTT ENSP00000449074.1:n.*1027-79_*1027-78insTTT
ENST00000549336.5:c.1025-79_1025-78insTTT ENSP00000449573.1:n.1025-79_1025-78insTTT
ENST00000550325.5:c.1175-79_1175-78insTTT ENSP00000447173.1:n.1175-79_1175-78insTTT
NM_000376.2:c.1025-79_1025-78insTTT NP_000367.1:n.1025-79_1025-78insTTT
NM_001017535.1:c.1025-79_1025-78insTTT NP_001017535.1:n.1025-79_1025-78insTTT
NM_001017536.1:c.1175-79_1175-78insTTT NP_001017536.1:n.1175-79_1175-78insTTT
XM_006719587.2:c.1025-79_1025-78insTTT XP_006719650.1:n.1025-79_1025-78insTTT
XM_011538720.1:c.1025-79_1025-78insTTT XP_011537022.1:n.1025-79_1025-78insTTT
NM_001364085.1:c.1025-79_1025-78insTTT NP_001351014.1:n.1025-79_1025-78insTTT
XM_006719587.3:c.1025-79_1025-78insTTT XP_006719650.1:n.1025-79_1025-78insTTT
XM_011538720.2:c.1025-79_1025-78insTTT XP_011537022.1:n.1025-79_1025-78insTTT
XM_024449178.1:c.1094-79_1094-78insTTT XP_024304946.1:n.1094-79_1094-78insTTT
NM_000376.3:c.1025-79_1025-78insTTT MANE Select NP_000367.1:n.1025-79_1025-78insTTT
NM_001017535.2:c.1025-79_1025-78insTTT NP_001017535.1:n.1025-79_1025-78insTTT
NM_001017536.2:c.1175-79_1175-78insTTT NP_001017536.1:n.1175-79_1175-78insTTT
NM_001364085.2:c.1025-79_1025-78insTTT NP_001351014.1:n.1025-79_1025-78insTTT
NM_001374661.1:c.1025-79_1025-78insTTT NP_001361590.1:n.1025-79_1025-78insTTT
NM_001374662.1:c.1025-79_1025-78insTTT NP_001361591.1:n.1025-79_1025-78insTTT