Canonical Allele Identifier: CA2034437728
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47892250_47892254delinsAACGT , CM000674.2:g.47892250_47892254delinsAACGT GRCh38
NC_000012.11:g.48286033_48286037delinsAACGT , CM000674.1:g.48286033_48286037delinsAACGT GRCh37
NC_000012.10:g.46572300_46572304delinsAACGT NCBI36
NG_008731.1:g.17778_17782delinsACGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000549336.6:c.-83-9480_-83-9476delinsACGTT MANE Select ENSP00000449573.2:n.-83-9480_-83-9476delinsACGTT
ENST00000229022.7:c.-84+7583_-84+7587delinsACGTT ENSP00000229022.3:n.-84+7583_-84+7587delinsACGTT
ENST00000395324.6:c.-83-9480_-83-9476delinsACGTT ENSP00000378734.2:n.-83-9480_-83-9476delinsACGTT
ENST00000546653.5:c.-3+7583_-3+7587delinsACGTT ENSP00000448659.1:n.-3+7583_-3+7587delinsACGTT
ENST00000547065.1:c.-3+12701_-3+12705delinsACGTT ENSP00000449074.1:n.-3+12701_-3+12705delinsACGTT
ENST00000548664.1:c.-84+7583_-84+7587delinsACGTT ENSP00000450105.1:n.-84+7583_-84+7587delinsACGTT
ENST00000549336.5:c.-83-9480_-83-9476delinsACGTT ENSP00000449573.1:n.-83-9480_-83-9476delinsACGTT
ENST00000550325.5:c.68-9480_68-9476delinsACGTT ENSP00000447173.1:n.68-9480_68-9476delinsACGTT
NM_000376.2:c.-83-9480_-83-9476delinsACGTT NP_000367.1:n.-83-9480_-83-9476delinsACGTT
NM_001017535.1:c.-84+7583_-84+7587delinsACGTT NP_001017535.1:n.-84+7583_-84+7587delinsACGTT
NM_001017536.1:c.68-9480_68-9476delinsACGTT NP_001017536.1:n.68-9480_68-9476delinsACGTT
XM_006719587.2:c.-3+12701_-3+12705delinsACGTT XP_006719650.1:n.-3+12701_-3+12705delinsACGTT
XM_011538720.1:c.-3+7583_-3+7587delinsACGTT XP_011537022.1:n.-3+7583_-3+7587delinsACGTT
NM_001364085.1:c.-83-9480_-83-9476delinsACGTT NP_001351014.1:n.-83-9480_-83-9476delinsACGTT
XM_006719587.3:c.-3+12701_-3+12705delinsACGTT XP_006719650.1:n.-3+12701_-3+12705delinsACGTT
XM_011538720.2:c.-3+7583_-3+7587delinsACGTT XP_011537022.1:n.-3+7583_-3+7587delinsACGTT
XM_024449178.1:c.67+12310_67+12314delinsACGTT XP_024304946.1:n.67+12310_67+12314delinsACGTT
NM_000376.3:c.-83-9480_-83-9476delinsACGTT MANE Select NP_000367.1:n.-83-9480_-83-9476delinsACGTT
NM_001017535.2:c.-84+7583_-84+7587delinsACGTT NP_001017535.1:n.-84+7583_-84+7587delinsACGTT
NM_001017536.2:c.68-9480_68-9476delinsACGTT NP_001017536.1:n.68-9480_68-9476delinsACGTT
NM_001364085.2:c.-83-9480_-83-9476delinsACGTT NP_001351014.1:n.-83-9480_-83-9476delinsACGTT
NM_001374661.1:c.-3+7583_-3+7587delinsACGTT NP_001361590.1:n.-3+7583_-3+7587delinsACGTT
NM_001374662.1:c.-3+12701_-3+12705delinsACGTT NP_001361591.1:n.-3+12701_-3+12705delinsACGTT