Canonical Allele Identifier: CA1828234458
Gene: VLDLR HGNC NCBI
VLDLR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2622270C= , CM000671.2:g.2622270C= GRCh38
NC_000009.11:g.2622270C= , CM000671.1:g.2622270C= GRCh37
NC_000009.10:g.2612270C= NCBI36
NG_012741.1:g.5478C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382096.6:c.81C= (VLDLR) ENSP00000371528.2:p.Thr27=
ENST00000382100.8:c.81C= (VLDLR) MANE Select ENSP00000371532.2:p.Thr27=
ENST00000679851.1:n.66C= (VLDLR)
ENST00000680243.1:c.81C= (VLDLR) ENSP00000505911.1:p.Thr27=
ENST00000680746.1:c.81C= (VLDLR) ENSP00000505030.1:p.Thr27=
ENST00000680891.1:c.81C= (VLDLR) ENSP00000505167.1:p.Thr27=
ENST00000681306.1:c.81C= (VLDLR) ENSP00000506072.1:p.Thr27=
ENST00000681618.1:c.81C= (VLDLR) ENSP00000505773.1:p.Thr27=
ENST00000681644.1:c.81C= (VLDLR) ENSP00000505180.1:p.Thr27=
ENST00000681770.1:n.69C= (VLDLR)
ENST00000681806.1:c.81C= (VLDLR) ENSP00000505282.1:p.Thr27=
ENST00000382096.5:c.81C= (VLDLR) ENSP00000371528.1:p.Thr27=
ENST00000382099.2:c.81C= (VLDLR) ENSP00000371531.2:p.Thr27=
ENST00000382100.7:c.81C= (VLDLR) ENSP00000371532.2:p.Thr27=
NM_001018056.1:c.81C= (VLDLR) NP_001018066.1:p.Thr27=
NM_003383.3:c.81C= (VLDLR) NP_003374.3:p.Thr27=
NR_015375.2:n.104G= (VLDLR-AS1)
XM_011518029.1:c.81C= (VLDLR) XP_011516331.1:p.Thr27=
NM_001018056.2:c.81C= (VLDLR) NP_001018066.1:p.Thr27=
NM_001322225.1:c.81C= (VLDLR) NP_001309154.1:p.Thr27=
NM_001322226.1:c.81C= (VLDLR) NP_001309155.1:p.Thr27=
NM_003383.4:c.81C= (VLDLR) NP_003374.3:p.Thr27=
XR_001746373.2:n.485C= (VLDLR)
XR_002956805.1:n.485C= (VLDLR)
NM_003383.5:c.81C= (VLDLR) MANE Select NP_003374.3:p.Thr27=
NM_001018056.3:c.81C= (VLDLR) NP_001018066.1:p.Thr27=
NM_001322225.2:c.81C= (VLDLR) NP_001309154.1:p.Thr27=
NM_001322226.2:c.81C= (VLDLR) NP_001309155.1:p.Thr27=