Canonical Allele Identifier: CA2618496281

Gene: VDR

Linked Data

• gnomAD v4: 12-47844512-TCAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47844519_47844522del , CM000674.2:g.47844519_47844522del	GRCh38
NC_000012.11:g.48238302_48238305del , CM000674.1:g.48238302_48238305del	GRCh37
NC_000012.10:g.46524569_46524572del	NCBI36
NG_008731.1:g.65516_65519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.*29_*32del	ENSP00000229022.5:n.*29_*32del
ENST00000549336.6:c.*230_*233del MANE Select	ENSP00000449573.2:n.*230_*233del
ENST00000229022.7:c.*230_*233del	ENSP00000229022.3:n.*230_*233del
ENST00000395324.6:c.*230_*233del	ENSP00000378734.2:n.*230_*233del
ENST00000547065.1:c.*1516_*1519del	ENSP00000449074.1:n.*1516_*1519del
ENST00000549336.5:c.*230_*233del	ENSP00000449573.1:n.*230_*233del
ENST00000550325.5:c.*230_*233del	ENSP00000447173.1:n.*230_*233del
NM_000376.2:c.*230_*233del	NP_000367.1:n.*230_*233del
NM_001017535.1:c.*230_*233del	NP_001017535.1:n.*230_*233del
NM_001017536.1:c.*230_*233del	NP_001017536.1:n.*230_*233del
XM_006719587.2:c.*230_*233del	XP_006719650.1:n.*230_*233del
XM_011538720.1:c.*230_*233del	XP_011537022.1:n.*230_*233del
NM_001364085.1:c.*29_*32del	NP_001351014.1:n.*29_*32del
NM_000376.3:c.*230_*233del MANE Select	NP_000367.1:n.*230_*233del
NM_001017535.2:c.*230_*233del	NP_001017535.1:n.*230_*233del
NM_001017536.2:c.*230_*233del	NP_001017536.1:n.*230_*233del
NM_001364085.2:c.*29_*32del	NP_001351014.1:n.*29_*32del
NM_001374661.1:c.*230_*233del	NP_001361590.1:n.*230_*233del
NM_001374662.1:c.*230_*233del	NP_001361591.1:n.*230_*233del