Canonical Allele Identifier: CA2034437709

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47892227_47892234delinsCCCATGCA , CM000674.2:g.47892227_47892234delinsCCCATGCA	GRCh38
NC_000012.11:g.48286010_48286017delinsCCCATGCA , CM000674.1:g.48286010_48286017delinsCCCATGCA	GRCh37
NC_000012.10:g.46572277_46572284delinsCCCATGCA	NCBI36
NG_008731.1:g.17798_17805delinsTGCATGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549336.6:c.-83-9460_-83-9453delinsTGCATGGG MANE Select	ENSP00000449573.2:n.-83-9460_-83-9453delinsTGCATGGG
ENST00000229022.7:c.-84+7603_-84+7610delinsTGCATGGG	ENSP00000229022.3:n.-84+7603_-84+7610delinsTGCATGGG
ENST00000395324.6:c.-83-9460_-83-9453delinsTGCATGGG	ENSP00000378734.2:n.-83-9460_-83-9453delinsTGCATGGG
ENST00000546653.5:c.-3+7603_-3+7610delinsTGCATGGG	ENSP00000448659.1:n.-3+7603_-3+7610delinsTGCATGGG
ENST00000547065.1:c.-3+12721_-3+12728delinsTGCATGGG	ENSP00000449074.1:n.-3+12721_-3+12728delinsTGCATGGG
ENST00000548664.1:c.-84+7603_-84+7610delinsTGCATGGG	ENSP00000450105.1:n.-84+7603_-84+7610delinsTGCATGGG
ENST00000549336.5:c.-83-9460_-83-9453delinsTGCATGGG	ENSP00000449573.1:n.-83-9460_-83-9453delinsTGCATGGG
ENST00000550325.5:c.68-9460_68-9453delinsTGCATGGG	ENSP00000447173.1:n.68-9460_68-9453delinsTGCATGGG
NM_000376.2:c.-83-9460_-83-9453delinsTGCATGGG	NP_000367.1:n.-83-9460_-83-9453delinsTGCATGGG
NM_001017535.1:c.-84+7603_-84+7610delinsTGCATGGG	NP_001017535.1:n.-84+7603_-84+7610delinsTGCATGGG
NM_001017536.1:c.68-9460_68-9453delinsTGCATGGG	NP_001017536.1:n.68-9460_68-9453delinsTGCATGGG
XM_006719587.2:c.-3+12721_-3+12728delinsTGCATGGG	XP_006719650.1:n.-3+12721_-3+12728delinsTGCATGGG
XM_011538720.1:c.-3+7603_-3+7610delinsTGCATGGG	XP_011537022.1:n.-3+7603_-3+7610delinsTGCATGGG
NM_001364085.1:c.-83-9460_-83-9453delinsTGCATGGG	NP_001351014.1:n.-83-9460_-83-9453delinsTGCATGGG
XM_006719587.3:c.-3+12721_-3+12728delinsTGCATGGG	XP_006719650.1:n.-3+12721_-3+12728delinsTGCATGGG
XM_011538720.2:c.-3+7603_-3+7610delinsTGCATGGG	XP_011537022.1:n.-3+7603_-3+7610delinsTGCATGGG
XM_024449178.1:c.67+12330_67+12337delinsTGCATGGG	XP_024304946.1:n.67+12330_67+12337delinsTGCATGGG
NM_000376.3:c.-83-9460_-83-9453delinsTGCATGGG MANE Select	NP_000367.1:n.-83-9460_-83-9453delinsTGCATGGG
NM_001017535.2:c.-84+7603_-84+7610delinsTGCATGGG	NP_001017535.1:n.-84+7603_-84+7610delinsTGCATGGG
NM_001017536.2:c.68-9460_68-9453delinsTGCATGGG	NP_001017536.1:n.68-9460_68-9453delinsTGCATGGG
NM_001364085.2:c.-83-9460_-83-9453delinsTGCATGGG	NP_001351014.1:n.-83-9460_-83-9453delinsTGCATGGG
NM_001374661.1:c.-3+7603_-3+7610delinsTGCATGGG	NP_001361590.1:n.-3+7603_-3+7610delinsTGCATGGG
NM_001374662.1:c.-3+12721_-3+12728delinsTGCATGGG	NP_001361591.1:n.-3+12721_-3+12728delinsTGCATGGG