Canonical Allele Identifier: CA1828245499
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2645640A= , CM000671.2:g.2645640A= GRCh38
NC_000009.11:g.2645640A= , CM000671.1:g.2645640A= GRCh37
NC_000009.10:g.2635640A= NCBI36
NG_012741.1:g.28848A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382099.3:c.937A=
ENST00000382100.8:c.1379A= MANE Select ENSP00000371532.2:p.Glu460=
ENST00000478776.2:n.824A=
ENST00000679718.1:n.615A=
ENST00000679750.1:n.795A=
ENST00000679851.1:n.1563A=
ENST00000680021.1:n.1579A=
ENST00000680043.1:c.931A=
ENST00000680219.1:c.946A=
ENST00000680243.1:c.*1158A= ENSP00000505911.1:n.*1158A=
ENST00000680296.1:c.805A=
ENST00000680332.1:n.462A=
ENST00000680746.1:c.1256A= ENSP00000505030.1:p.Glu419=
ENST00000680751.1:n.784A=
ENST00000680891.1:c.*1171A= ENSP00000505167.1:n.*1171A=
ENST00000680975.1:n.764A=
ENST00000681087.1:n.824A=
ENST00000681306.1:c.1379A= ENSP00000506072.1:p.Glu460=
ENST00000681618.1:c.1256A= ENSP00000505773.1:p.Glu419=
ENST00000681644.1:c.*1051A= ENSP00000505180.1:n.*1051A=
ENST00000681806.1:c.1379A= ENSP00000505282.1:p.Glu460=
ENST00000681942.1:c.927A=
ENST00000382099.2:c.1379A= ENSP00000371531.2:p.Glu460=
ENST00000382100.7:c.1379A= ENSP00000371532.2:p.Glu460=
NM_001018056.1:c.1379A= NP_001018066.1:p.Glu460=
NM_003383.3:c.1379A= NP_003374.3:p.Glu460=
XM_011518029.1:c.1256A= XP_011516331.1:p.Glu419=
NM_001018056.2:c.1379A= NP_001018066.1:p.Glu460=
NM_001322225.1:c.1256A= NP_001309154.1:p.Glu419=
NM_001322226.1:c.1256A= NP_001309155.1:p.Glu419=
NM_003383.4:c.1379A= NP_003374.3:p.Glu460=
XR_001746373.2:n.1783A=
XR_002956805.1:n.1783A=
NM_003383.5:c.1379A= MANE Select NP_003374.3:p.Glu460=
NM_001018056.3:c.1379A= NP_001018066.1:p.Glu460=
NM_001322225.2:c.1256A= NP_001309154.1:p.Glu419=
NM_001322226.2:c.1256A= NP_001309155.1:p.Glu419=