Canonical Allele Identifier: CA479696489

Gene: VDR

Linked Data

• MyVariant Identifiers: chr12:g.48238643C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47844860C>G , CM000674.2:g.47844860C>G	GRCh38
NC_000012.11:g.48238643C>G , CM000674.1:g.48238643C>G	GRCh37
NC_000012.10:g.46524910C>G	NCBI36
NG_008731.1:g.65172G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.1170G>C	ENSP00000229022.5:p.Leu390=
ENST00000549336.6:c.1170G>C MANE Select	ENSP00000449573.2:p.Leu390=
ENST00000229022.7:c.1170G>C	ENSP00000229022.3:p.Leu390=
ENST00000395324.6:c.1170G>C	ENSP00000378734.2:p.Leu390=
ENST00000547065.1:c.*1172G>C	ENSP00000449074.1:n.*1172G>C
ENST00000549336.5:c.1170G>C	ENSP00000449573.1:p.Leu390=
ENST00000550325.5:c.1320G>C	ENSP00000447173.1:p.Leu440=
NM_000376.2:c.1170G>C	NP_000367.1:p.Leu390=
NM_001017535.1:c.1170G>C	NP_001017535.1:p.Leu390=
NM_001017536.1:c.1320G>C	NP_001017536.1:p.Leu440=
XM_006719587.2:c.1170G>C	XP_006719650.1:p.Leu390=
XM_011538720.1:c.1170G>C	XP_011537022.1:p.Leu390=
NM_001364085.1:c.1170G>C	NP_001351014.1:p.Leu390=
XM_006719587.3:c.1170G>C	XP_006719650.1:p.Leu390=
XM_011538720.2:c.1170G>C	XP_011537022.1:p.Leu390=
XM_024449178.1:c.1239G>C	XP_024304946.1:p.Leu413=
NM_000376.3:c.1170G>C MANE Select	NP_000367.1:p.Leu390=
NM_001017535.2:c.1170G>C	NP_001017535.1:p.Leu390=
NM_001017536.2:c.1320G>C	NP_001017536.1:p.Leu440=
NM_001364085.2:c.1170G>C	NP_001351014.1:p.Leu390=
NM_001374661.1:c.1170G>C	NP_001361590.1:p.Leu390=
NM_001374662.1:c.1170G>C	NP_001361591.1:p.Leu390=