Canonical Allele Identifier: CA1828245037
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2644736A= , CM000671.2:g.2644736A= GRCh38
NC_000009.11:g.2644736A= , CM000671.1:g.2644736A= GRCh37
NC_000009.10:g.2634736A= NCBI36
NG_012741.1:g.27944A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382099.3:c.627A=
ENST00000382100.8:c.1069A= MANE Select ENSP00000371532.2:p.Ile357=
ENST00000478776.2:n.411A=
ENST00000679718.1:n.202A=
ENST00000679750.1:n.382A=
ENST00000679851.1:n.1150A=
ENST00000680021.1:n.1269A=
ENST00000680043.1:c.621A=
ENST00000680150.1:n.249A=
ENST00000680219.1:c.621A=
ENST00000680243.1:c.*848A= ENSP00000505911.1:n.*848A=
ENST00000680296.1:c.621A=
ENST00000680332.1:n.49A=
ENST00000680746.1:c.946A= ENSP00000505030.1:p.Ile316=
ENST00000680751.1:n.371A=
ENST00000680891.1:c.*861A= ENSP00000505167.1:n.*861A=
ENST00000680975.1:n.351A=
ENST00000681087.1:n.411A=
ENST00000681306.1:c.1069A= ENSP00000506072.1:p.Ile357=
ENST00000681618.1:c.946A= ENSP00000505773.1:p.Ile316=
ENST00000681644.1:c.*741A= ENSP00000505180.1:n.*741A=
ENST00000681806.1:c.1069A= ENSP00000505282.1:p.Ile357=
ENST00000681942.1:c.621A=
ENST00000382099.2:c.1069A= ENSP00000371531.2:p.Ile357=
ENST00000382100.7:c.1069A= ENSP00000371532.2:p.Ile357=
NM_001018056.1:c.1069A= NP_001018066.1:p.Ile357=
NM_003383.3:c.1069A= NP_003374.3:p.Ile357=
XM_011518029.1:c.946A= XP_011516331.1:p.Ile316=
NM_001018056.2:c.1069A= NP_001018066.1:p.Ile357=
NM_001322225.1:c.946A= NP_001309154.1:p.Ile316=
NM_001322226.1:c.946A= NP_001309155.1:p.Ile316=
NM_003383.4:c.1069A= NP_003374.3:p.Ile357=
XR_001746373.2:n.1473A=
XR_002956805.1:n.1473A=
NM_003383.5:c.1069A= MANE Select NP_003374.3:p.Ile357=
NM_001018056.3:c.1069A= NP_001018066.1:p.Ile357=
NM_001322225.2:c.946A= NP_001309154.1:p.Ile316=
NM_001322226.2:c.946A= NP_001309155.1:p.Ile316=