Canonical Allele Identifier: CA2034416907

Gene: VDR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47862137_47862138delinsTG , CM000674.2:g.47862137_47862138delinsTG	GRCh38
NC_000012.11:g.48255920_48255921delinsTG , CM000674.1:g.48255920_48255921delinsTG	GRCh37
NC_000012.10:g.46542187_46542188delinsTG	NCBI36
NG_008731.1:g.47894_47895delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.277+2909_277+2910delinsCA	ENSP00000229022.5:n.277+2909_277+2910delinsCA
ENST00000549336.6:c.277+2909_277+2910delinsCA MANE Select	ENSP00000449573.2:n.277+2909_277+2910delinsCA
ENST00000229022.7:c.277+2909_277+2910delinsCA	ENSP00000229022.3:n.277+2909_277+2910delinsCA
ENST00000395324.6:c.277+2909_277+2910delinsCA	ENSP00000378734.2:n.277+2909_277+2910delinsCA
ENST00000546653.5:c.277+2909_277+2910delinsCA	ENSP00000448659.1:n.277+2909_277+2910delinsCA
ENST00000547065.1:c.*279+2909_*279+2910delinsCA	ENSP00000449074.1:n.*279+2909_*279+2910delinsCA
ENST00000548664.1:c.277+2909_277+2910delinsCA	ENSP00000450105.1:n.277+2909_277+2910delinsCA
ENST00000549336.5:c.277+2909_277+2910delinsCA	ENSP00000449573.1:n.277+2909_277+2910delinsCA
ENST00000550314.5:c.277+2909_277+2910delinsCA	ENSP00000449561.1:n.277+2909_277+2910delinsCA
ENST00000550325.5:c.427+2909_427+2910delinsCA	ENSP00000447173.1:n.427+2909_427+2910delinsCA
NM_000376.2:c.277+2909_277+2910delinsCA	NP_000367.1:n.277+2909_277+2910delinsCA
NM_001017535.1:c.277+2909_277+2910delinsCA	NP_001017535.1:n.277+2909_277+2910delinsCA
NM_001017536.1:c.427+2909_427+2910delinsCA	NP_001017536.1:n.427+2909_427+2910delinsCA
XM_006719587.2:c.277+2909_277+2910delinsCA	XP_006719650.1:n.277+2909_277+2910delinsCA
XM_011538720.1:c.277+2909_277+2910delinsCA	XP_011537022.1:n.277+2909_277+2910delinsCA
NM_001364085.1:c.277+2909_277+2910delinsCA	NP_001351014.1:n.277+2909_277+2910delinsCA
XM_006719587.3:c.277+2909_277+2910delinsCA	XP_006719650.1:n.277+2909_277+2910delinsCA
XM_011538720.2:c.277+2909_277+2910delinsCA	XP_011537022.1:n.277+2909_277+2910delinsCA
XM_024449178.1:c.346+2909_346+2910delinsCA	XP_024304946.1:n.346+2909_346+2910delinsCA
NM_000376.3:c.277+2909_277+2910delinsCA MANE Select	NP_000367.1:n.277+2909_277+2910delinsCA
NM_001017535.2:c.277+2909_277+2910delinsCA	NP_001017535.1:n.277+2909_277+2910delinsCA
NM_001017536.2:c.427+2909_427+2910delinsCA	NP_001017536.1:n.427+2909_427+2910delinsCA
NM_001364085.2:c.277+2909_277+2910delinsCA	NP_001351014.1:n.277+2909_277+2910delinsCA
NM_001374661.1:c.277+2909_277+2910delinsCA	NP_001361590.1:n.277+2909_277+2910delinsCA
NM_001374662.1:c.277+2909_277+2910delinsCA	NP_001361591.1:n.277+2909_277+2910delinsCA