Canonical Allele Identifier: CA947337769

Gene: VDR

Linked Data

• gnomAD v3: 12-47891892-A-ACCCCCCCCCCCCCCCCCC
• gnomAD v4: 12-47891892-A-ACCCCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47891894_47891895insCCCCCCCCCCCCCCCCCC , CM000674.2:g.47891894_47891895insCCCCCCCCCCCCCCCCCC	GRCh38
NC_000012.11:g.48285677_48285678insCCCCCCCCCCCCCCCCCC , CM000674.1:g.48285677_48285678insCCCCCCCCCCCCCCCCCC	GRCh37
NC_000012.10:g.46571944_46571945insCCCCCCCCCCCCCCCCCC	NCBI36
NG_008731.1:g.18139_18140insGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549336.6:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000449573.2:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
ENST00000229022.7:c.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG	ENSP00000229022.3:n.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG
ENST00000395324.6:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG	ENSP00000378734.2:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
ENST00000546653.5:c.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG	ENSP00000448659.1:n.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG
ENST00000547065.1:c.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG	ENSP00000449074.1:n.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG
ENST00000548664.1:c.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG	ENSP00000450105.1:n.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG
ENST00000549336.5:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG	ENSP00000449573.1:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
ENST00000550325.5:c.68-9119_68-9118insGGGGGGGGGGGGGGGGGG	ENSP00000447173.1:n.68-9119_68-9118insGGGGGGGGGGGGGGGGGG
NM_000376.2:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG	NP_000367.1:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
NM_001017535.1:c.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG	NP_001017535.1:n.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG
NM_001017536.1:c.68-9119_68-9118insGGGGGGGGGGGGGGGGGG	NP_001017536.1:n.68-9119_68-9118insGGGGGGGGGGGGGGGGGG
XM_006719587.2:c.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG	XP_006719650.1:n.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG
XM_011538720.1:c.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG	XP_011537022.1:n.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG
NM_001364085.1:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG	NP_001351014.1:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
XM_006719587.3:c.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG	XP_006719650.1:n.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG
XM_011538720.2:c.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG	XP_011537022.1:n.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG
XM_024449178.1:c.67+12671_67+12672insGGGGGGGGGGGGGGGGGG	XP_024304946.1:n.67+12671_67+12672insGGGGGGGGGGGGGGGGGG
NM_000376.3:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG MANE Select	NP_000367.1:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
NM_001017535.2:c.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG	NP_001017535.1:n.-84+7944_-84+7945insGGGGGGGGGGGGGGGGGG
NM_001017536.2:c.68-9119_68-9118insGGGGGGGGGGGGGGGGGG	NP_001017536.1:n.68-9119_68-9118insGGGGGGGGGGGGGGGGGG
NM_001364085.2:c.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG	NP_001351014.1:n.-83-9119_-83-9118insGGGGGGGGGGGGGGGGGG
NM_001374661.1:c.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG	NP_001361590.1:n.-3+7944_-3+7945insGGGGGGGGGGGGGGGGGG
NM_001374662.1:c.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG	NP_001361591.1:n.-2-12778_-2-12777insGGGGGGGGGGGGGGGGGG