Canonical Allele Identifier: CA372785740

Gene: VLDLR VLDLR-AS1

Linked Data

• gnomAD v4: 9-2622230-C-T
• MyVariant Identifiers: chr9:g.2622230C>T (hg19) ; chr9:g.2622230C>T (hg38)

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