Canonical Allele Identifier: CA1828245489
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2645622T= , CM000671.2:g.2645622T= GRCh38
NC_000009.11:g.2645622T= , CM000671.1:g.2645622T= GRCh37
NC_000009.10:g.2635622T= NCBI36
NG_012741.1:g.28830T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382099.3:c.919T=
ENST00000382100.8:c.1361T= MANE Select ENSP00000371532.2:p.Ile454=
ENST00000478776.2:n.806T=
ENST00000679718.1:n.597T=
ENST00000679750.1:n.777T=
ENST00000679851.1:n.1545T=
ENST00000680021.1:n.1561T=
ENST00000680043.1:c.913T=
ENST00000680219.1:c.928T=
ENST00000680243.1:c.*1140T= ENSP00000505911.1:n.*1140T=
ENST00000680296.1:c.787T=
ENST00000680332.1:n.444T=
ENST00000680746.1:c.1238T= ENSP00000505030.1:p.Ile413=
ENST00000680751.1:n.766T=
ENST00000680891.1:c.*1153T= ENSP00000505167.1:n.*1153T=
ENST00000680975.1:n.746T=
ENST00000681087.1:n.806T=
ENST00000681306.1:c.1361T= ENSP00000506072.1:p.Ile454=
ENST00000681618.1:c.1238T= ENSP00000505773.1:p.Ile413=
ENST00000681644.1:c.*1033T= ENSP00000505180.1:n.*1033T=
ENST00000681806.1:c.1361T= ENSP00000505282.1:p.Ile454=
ENST00000681942.1:c.909T=
ENST00000382099.2:c.1361T= ENSP00000371531.2:p.Ile454=
ENST00000382100.7:c.1361T= ENSP00000371532.2:p.Ile454=
NM_001018056.1:c.1361T= NP_001018066.1:p.Ile454=
NM_003383.3:c.1361T= NP_003374.3:p.Ile454=
XM_011518029.1:c.1238T= XP_011516331.1:p.Ile413=
NM_001018056.2:c.1361T= NP_001018066.1:p.Ile454=
NM_001322225.1:c.1238T= NP_001309154.1:p.Ile413=
NM_001322226.1:c.1238T= NP_001309155.1:p.Ile413=
NM_003383.4:c.1361T= NP_003374.3:p.Ile454=
XR_001746373.2:n.1765T=
XR_002956805.1:n.1765T=
NM_003383.5:c.1361T= MANE Select NP_003374.3:p.Ile454=
NM_001018056.3:c.1361T= NP_001018066.1:p.Ile454=
NM_001322225.2:c.1238T= NP_001309154.1:p.Ile413=
NM_001322226.2:c.1238T= NP_001309155.1:p.Ile413=