Canonical Allele Identifier: CA384513536

Gene: VDR

Linked Data

• MyVariant Identifiers: chr12:g.48238536A>G (hg19) ; chr12:g.47844753A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47844753A>G , CM000674.2:g.47844753A>G	GRCh38
NC_000012.11:g.48238536A>G , CM000674.1:g.48238536A>G	GRCh37
NC_000012.10:g.46524803A>G	NCBI36
NG_008731.1:g.65279T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229022.9:c.1277T>C	ENSP00000229022.5:p.Ile426Thr
ENST00000549336.6:c.1277T>C MANE Select	ENSP00000449573.2:p.Ile426Thr
ENST00000229022.7:c.1277T>C	ENSP00000229022.3:p.Ile426Thr
ENST00000395324.6:c.1277T>C	ENSP00000378734.2:p.Ile426Thr
ENST00000547065.1:c.*1279T>C	ENSP00000449074.1:n.*1279T>C
ENST00000549336.5:c.1277T>C	ENSP00000449573.1:p.Ile426Thr
ENST00000550325.5:c.1427T>C	ENSP00000447173.1:p.Ile476Thr
NM_000376.2:c.1277T>C	NP_000367.1:p.Ile426Thr
NM_001017535.1:c.1277T>C	NP_001017535.1:p.Ile426Thr
NM_001017536.1:c.1427T>C	NP_001017536.1:p.Ile476Thr
XM_006719587.2:c.1277T>C	XP_006719650.1:p.Ile426Thr
XM_011538720.1:c.1277T>C	XP_011537022.1:p.Ile426Thr
NM_001364085.1:c.1277T>C	NP_001351014.1:p.Ile426Thr
XM_006719587.3:c.1277T>C	XP_006719650.1:p.Ile426Thr
XM_011538720.2:c.1277T>C	XP_011537022.1:p.Ile426Thr
XM_024449178.1:c.1346T>C	XP_024304946.1:p.Ile449Thr
NM_000376.3:c.1277T>C MANE Select	NP_000367.1:p.Ile426Thr
NM_001017535.2:c.1277T>C	NP_001017535.1:p.Ile426Thr
NM_001017536.2:c.1427T>C	NP_001017536.1:p.Ile476Thr
NM_001364085.2:c.1277T>C	NP_001351014.1:p.Ile426Thr
NM_001374661.1:c.1277T>C	NP_001361590.1:p.Ile426Thr
NM_001374662.1:c.1277T>C	NP_001361591.1:p.Ile426Thr