Canonical Allele Identifier: CA2034408971
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47844896C= , CM000674.2:g.47844896C= GRCh38
NC_000012.11:g.48238679C= , CM000674.1:g.48238679C= GRCh37
NC_000012.10:g.46524946C= NCBI36
NG_008731.1:g.65136G=

Transcript Alleles

HGVS Amino-acid change
ENST00000229022.9:c.1134G= ENSP00000229022.5:p.Leu378=
ENST00000549336.6:c.1134G= MANE Select ENSP00000449573.2:p.Leu378=
ENST00000229022.7:c.1134G= ENSP00000229022.3:p.Leu378=
ENST00000395324.6:c.1134G= ENSP00000378734.2:p.Leu378=
ENST00000547065.1:c.*1136G= ENSP00000449074.1:n.*1136G=
ENST00000549336.5:c.1134G= ENSP00000449573.1:p.Leu378=
ENST00000550325.5:c.1284G= ENSP00000447173.1:p.Leu428=
NM_000376.2:c.1134G= NP_000367.1:p.Leu378=
NM_001017535.1:c.1134G= NP_001017535.1:p.Leu378=
NM_001017536.1:c.1284G= NP_001017536.1:p.Leu428=
XM_006719587.2:c.1134G= XP_006719650.1:p.Leu378=
XM_011538720.1:c.1134G= XP_011537022.1:p.Leu378=
NM_001364085.1:c.1134G= NP_001351014.1:p.Leu378=
XM_006719587.3:c.1134G= XP_006719650.1:p.Leu378=
XM_011538720.2:c.1134G= XP_011537022.1:p.Leu378=
XM_024449178.1:c.1203G= XP_024304946.1:p.Leu401=
NM_000376.3:c.1134G= MANE Select NP_000367.1:p.Leu378=
NM_001017535.2:c.1134G= NP_001017535.1:p.Leu378=
NM_001017536.2:c.1284G= NP_001017536.1:p.Leu428=
NM_001364085.2:c.1134G= NP_001351014.1:p.Leu378=
NM_001374661.1:c.1134G= NP_001361590.1:p.Leu378=
NM_001374662.1:c.1134G= NP_001361591.1:p.Leu378=