Canonical Allele Identifier: CA372785740
Gene: VLDLR HGNC NCBI
VLDLR-AS1 HGNC NCBI

Linked Data

gnomAD v4: 9-2622230-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2622230C>T , CM000671.2:g.2622230C>T GRCh38
NC_000009.11:g.2622230C>T , CM000671.1:g.2622230C>T GRCh37
NC_000009.10:g.2612230C>T NCBI36
NG_012741.1:g.5438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382096.6:c.41C>T (VLDLR) ENSP00000371528.2:p.Ala14Val
ENST00000382100.8:c.41C>T (VLDLR) MANE Select ENSP00000371532.2:p.Ala14Val
ENST00000679851.1:n.26C>T (VLDLR)
ENST00000680243.1:c.41C>T (VLDLR) ENSP00000505911.1:p.Ala14Val
ENST00000680746.1:c.41C>T (VLDLR) ENSP00000505030.1:p.Ala14Val
ENST00000680891.1:c.41C>T (VLDLR) ENSP00000505167.1:p.Ala14Val
ENST00000681306.1:c.41C>T (VLDLR) ENSP00000506072.1:p.Ala14Val
ENST00000681618.1:c.41C>T (VLDLR) ENSP00000505773.1:p.Ala14Val
ENST00000681644.1:c.41C>T (VLDLR) ENSP00000505180.1:p.Ala14Val
ENST00000681770.1:n.29C>T (VLDLR)
ENST00000681806.1:c.41C>T (VLDLR) ENSP00000505282.1:p.Ala14Val
ENST00000382096.5:c.41C>T (VLDLR) ENSP00000371528.1:p.Ala14Val
ENST00000382099.2:c.41C>T (VLDLR) ENSP00000371531.2:p.Ala14Val
ENST00000382100.7:c.41C>T (VLDLR) ENSP00000371532.2:p.Ala14Val
NM_001018056.1:c.41C>T (VLDLR) NP_001018066.1:p.Ala14Val
NM_003383.3:c.41C>T (VLDLR) NP_003374.3:p.Ala14Val
NR_015375.2:n.144G>A (VLDLR-AS1)
XM_011518029.1:c.41C>T (VLDLR) XP_011516331.1:p.Ala14Val
NM_001018056.2:c.41C>T (VLDLR) NP_001018066.1:p.Ala14Val
NM_001322225.1:c.41C>T (VLDLR) NP_001309154.1:p.Ala14Val
NM_001322226.1:c.41C>T (VLDLR) NP_001309155.1:p.Ala14Val
NM_003383.4:c.41C>T (VLDLR) NP_003374.3:p.Ala14Val
XR_001746373.2:n.445C>T (VLDLR)
XR_002956805.1:n.445C>T (VLDLR)
NM_003383.5:c.41C>T (VLDLR) MANE Select NP_003374.3:p.Ala14Val
NM_001018056.3:c.41C>T (VLDLR) NP_001018066.1:p.Ala14Val
NM_001322225.2:c.41C>T (VLDLR) NP_001309154.1:p.Ala14Val
NM_001322226.2:c.41C>T (VLDLR) NP_001309155.1:p.Ala14Val