Canonical Allele Identifier: CA2795869781

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47891907_47891908insCCCCCCCCCCC , CM000674.2:g.47891907_47891908insCCCCCCCCCCC	GRCh38
NC_000012.11:g.48285690_48285691insCCCCCCCCCCC , CM000674.1:g.48285690_48285691insCCCCCCCCCCC	GRCh37
NC_000012.10:g.46571957_46571958insCCCCCCCCCCC	NCBI36
NG_008731.1:g.18129_18130insGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549336.6:c.-83-9129_-83-9128insGGGGGGGGGGG MANE Select	ENSP00000449573.2:n.-83-9129_-83-9128insGGGGGGGGGGG
ENST00000229022.7:c.-84+7934_-84+7935insGGGGGGGGGGG	ENSP00000229022.3:n.-84+7934_-84+7935insGGGGGGGGGGG
ENST00000395324.6:c.-83-9129_-83-9128insGGGGGGGGGGG	ENSP00000378734.2:n.-83-9129_-83-9128insGGGGGGGGGGG
ENST00000546653.5:c.-3+7934_-3+7935insGGGGGGGGGGG	ENSP00000448659.1:n.-3+7934_-3+7935insGGGGGGGGGGG
ENST00000547065.1:c.-2-12788_-2-12787insGGGGGGGGGGG	ENSP00000449074.1:n.-2-12788_-2-12787insGGGGGGGGGGG
ENST00000548664.1:c.-84+7934_-84+7935insGGGGGGGGGGG	ENSP00000450105.1:n.-84+7934_-84+7935insGGGGGGGGGGG
ENST00000549336.5:c.-83-9129_-83-9128insGGGGGGGGGGG	ENSP00000449573.1:n.-83-9129_-83-9128insGGGGGGGGGGG
ENST00000550325.5:c.68-9129_68-9128insGGGGGGGGGGG	ENSP00000447173.1:n.68-9129_68-9128insGGGGGGGGGGG
NM_000376.2:c.-83-9129_-83-9128insGGGGGGGGGGG	NP_000367.1:n.-83-9129_-83-9128insGGGGGGGGGGG
NM_001017535.1:c.-84+7934_-84+7935insGGGGGGGGGGG	NP_001017535.1:n.-84+7934_-84+7935insGGGGGGGGGGG
NM_001017536.1:c.68-9129_68-9128insGGGGGGGGGGG	NP_001017536.1:n.68-9129_68-9128insGGGGGGGGGGG
XM_006719587.2:c.-2-12788_-2-12787insGGGGGGGGGGG	XP_006719650.1:n.-2-12788_-2-12787insGGGGGGGGGGG
XM_011538720.1:c.-3+7934_-3+7935insGGGGGGGGGGG	XP_011537022.1:n.-3+7934_-3+7935insGGGGGGGGGGG
NM_001364085.1:c.-83-9129_-83-9128insGGGGGGGGGGG	NP_001351014.1:n.-83-9129_-83-9128insGGGGGGGGGGG
XM_006719587.3:c.-2-12788_-2-12787insGGGGGGGGGGG	XP_006719650.1:n.-2-12788_-2-12787insGGGGGGGGGGG
XM_011538720.2:c.-3+7934_-3+7935insGGGGGGGGGGG	XP_011537022.1:n.-3+7934_-3+7935insGGGGGGGGGGG
XM_024449178.1:c.67+12661_67+12662insGGGGGGGGGGG	XP_024304946.1:n.67+12661_67+12662insGGGGGGGGGGG
NM_000376.3:c.-83-9129_-83-9128insGGGGGGGGGGG MANE Select	NP_000367.1:n.-83-9129_-83-9128insGGGGGGGGGGG
NM_001017535.2:c.-84+7934_-84+7935insGGGGGGGGGGG	NP_001017535.1:n.-84+7934_-84+7935insGGGGGGGGGGG
NM_001017536.2:c.68-9129_68-9128insGGGGGGGGGGG	NP_001017536.1:n.68-9129_68-9128insGGGGGGGGGGG
NM_001364085.2:c.-83-9129_-83-9128insGGGGGGGGGGG	NP_001351014.1:n.-83-9129_-83-9128insGGGGGGGGGGG
NM_001374661.1:c.-3+7934_-3+7935insGGGGGGGGGGG	NP_001361590.1:n.-3+7934_-3+7935insGGGGGGGGGGG
NM_001374662.1:c.-2-12788_-2-12787insGGGGGGGGGGG	NP_001361591.1:n.-2-12788_-2-12787insGGGGGGGGGGG