Canonical Allele Identifier: CA1828245035
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2644733G= , CM000671.2:g.2644733G= GRCh38
NC_000009.11:g.2644733G= , CM000671.1:g.2644733G= GRCh37
NC_000009.10:g.2634733G= NCBI36
NG_012741.1:g.27941G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382099.3:c.625-1G=
ENST00000382100.8:c.1067-1G= MANE Select ENSP00000371532.2:n.1067-1G=
ENST00000478776.2:n.408G=
ENST00000679718.1:n.199G=
ENST00000679750.1:n.379G=
ENST00000679851.1:n.1148-1G=
ENST00000680021.1:n.1267-1G=
ENST00000680043.1:c.619-1G=
ENST00000680150.1:n.247-1G=
ENST00000680219.1:c.619-1G=
ENST00000680243.1:c.*846-1G= ENSP00000505911.1:n.*846-1G=
ENST00000680296.1:c.619-1G=
ENST00000680332.1:n.46G=
ENST00000680746.1:c.944-1G= ENSP00000505030.1:n.944-1G=
ENST00000680751.1:n.368G=
ENST00000680891.1:c.*859-1G= ENSP00000505167.1:n.*859-1G=
ENST00000680975.1:n.348G=
ENST00000681087.1:n.408G=
ENST00000681306.1:c.1067-1G= ENSP00000506072.1:n.1067-1G=
ENST00000681618.1:c.944-1G= ENSP00000505773.1:n.944-1G=
ENST00000681644.1:c.*739-1G= ENSP00000505180.1:n.*739-1G=
ENST00000681806.1:c.1067-1G= ENSP00000505282.1:n.1067-1G=
ENST00000681942.1:c.619-1G=
ENST00000382099.2:c.1067-1G= ENSP00000371531.2:n.1067-1G=
ENST00000382100.7:c.1067-1G= ENSP00000371532.2:n.1067-1G=
NM_001018056.1:c.1067-1G= NP_001018066.1:n.1067-1G=
NM_003383.3:c.1067-1G= NP_003374.3:n.1067-1G=
XM_011518029.1:c.944-1G= XP_011516331.1:n.944-1G=
NM_001018056.2:c.1067-1G= NP_001018066.1:n.1067-1G=
NM_001322225.1:c.944-1G= NP_001309154.1:n.944-1G=
NM_001322226.1:c.944-1G= NP_001309155.1:n.944-1G=
NM_003383.4:c.1067-1G= NP_003374.3:n.1067-1G=
XR_001746373.2:n.1471-1G=
XR_002956805.1:n.1471-1G=
NM_003383.5:c.1067-1G= MANE Select NP_003374.3:n.1067-1G=
NM_001018056.3:c.1067-1G= NP_001018066.1:n.1067-1G=
NM_001322225.2:c.944-1G= NP_001309154.1:n.944-1G=
NM_001322226.2:c.944-1G= NP_001309155.1:n.944-1G=