Canonical Allele Identifier: CA2795869776

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47891891_47891892insCCCCCCCCCCCCCCC , CM000674.2:g.47891891_47891892insCCCCCCCCCCCCCCC	GRCh38
NC_000012.11:g.48285674_48285675insCCCCCCCCCCCCCCC , CM000674.1:g.48285674_48285675insCCCCCCCCCCCCCCC	GRCh37
NC_000012.10:g.46571941_46571942insCCCCCCCCCCCCCCC	NCBI36
NG_008731.1:g.18142_18143insGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549336.6:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG MANE Select	ENSP00000449573.2:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
ENST00000229022.7:c.-84+7947_-84+7948insGGGGGGGGGGGGGGG	ENSP00000229022.3:n.-84+7947_-84+7948insGGGGGGGGGGGGGGG
ENST00000395324.6:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG	ENSP00000378734.2:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
ENST00000546653.5:c.-3+7947_-3+7948insGGGGGGGGGGGGGGG	ENSP00000448659.1:n.-3+7947_-3+7948insGGGGGGGGGGGGGGG
ENST00000547065.1:c.-2-12775_-2-12774insGGGGGGGGGGGGGGG	ENSP00000449074.1:n.-2-12775_-2-12774insGGGGGGGGGGGGGGG
ENST00000548664.1:c.-84+7947_-84+7948insGGGGGGGGGGGGGGG	ENSP00000450105.1:n.-84+7947_-84+7948insGGGGGGGGGGGGGGG
ENST00000549336.5:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG	ENSP00000449573.1:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
ENST00000550325.5:c.68-9116_68-9115insGGGGGGGGGGGGGGG	ENSP00000447173.1:n.68-9116_68-9115insGGGGGGGGGGGGGGG
NM_000376.2:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG	NP_000367.1:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
NM_001017535.1:c.-84+7947_-84+7948insGGGGGGGGGGGGGGG	NP_001017535.1:n.-84+7947_-84+7948insGGGGGGGGGGGGGGG
NM_001017536.1:c.68-9116_68-9115insGGGGGGGGGGGGGGG	NP_001017536.1:n.68-9116_68-9115insGGGGGGGGGGGGGGG
XM_006719587.2:c.-2-12775_-2-12774insGGGGGGGGGGGGGGG	XP_006719650.1:n.-2-12775_-2-12774insGGGGGGGGGGGGGGG
XM_011538720.1:c.-3+7947_-3+7948insGGGGGGGGGGGGGGG	XP_011537022.1:n.-3+7947_-3+7948insGGGGGGGGGGGGGGG
NM_001364085.1:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG	NP_001351014.1:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
XM_006719587.3:c.-2-12775_-2-12774insGGGGGGGGGGGGGGG	XP_006719650.1:n.-2-12775_-2-12774insGGGGGGGGGGGGGGG
XM_011538720.2:c.-3+7947_-3+7948insGGGGGGGGGGGGGGG	XP_011537022.1:n.-3+7947_-3+7948insGGGGGGGGGGGGGGG
XM_024449178.1:c.67+12674_67+12675insGGGGGGGGGGGGGGG	XP_024304946.1:n.67+12674_67+12675insGGGGGGGGGGGGGGG
NM_000376.3:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG MANE Select	NP_000367.1:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
NM_001017535.2:c.-84+7947_-84+7948insGGGGGGGGGGGGGGG	NP_001017535.1:n.-84+7947_-84+7948insGGGGGGGGGGGGGGG
NM_001017536.2:c.68-9116_68-9115insGGGGGGGGGGGGGGG	NP_001017536.1:n.68-9116_68-9115insGGGGGGGGGGGGGGG
NM_001364085.2:c.-83-9116_-83-9115insGGGGGGGGGGGGGGG	NP_001351014.1:n.-83-9116_-83-9115insGGGGGGGGGGGGGGG
NM_001374661.1:c.-3+7947_-3+7948insGGGGGGGGGGGGGGG	NP_001361590.1:n.-3+7947_-3+7948insGGGGGGGGGGGGGGG
NM_001374662.1:c.-2-12775_-2-12774insGGGGGGGGGGGGGGG	NP_001361591.1:n.-2-12775_-2-12774insGGGGGGGGGGGGGGG