Canonical Allele Identifier: CA2689246405

Gene: VLDLR

Linked Data

• gnomAD v4: 9-2643029-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643029C>A , CM000671.2:g.2643029C>A	GRCh38
NC_000009.11:g.2643029C>A , CM000671.1:g.2643029C>A	GRCh37
NC_000009.10:g.2633029C>A	NCBI36
NG_012741.1:g.26237C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382100.8:c.449-131C>A MANE Select	ENSP00000371532.2:n.449-131C>A
ENST00000679851.1:n.434-131C>A
ENST00000680021.1:n.649-131C>A
ENST00000680243.1:c.*228-131C>A	ENSP00000505911.1:n.*228-131C>A
ENST00000680746.1:c.326-131C>A	ENSP00000505030.1:n.326-131C>A
ENST00000680891.1:c.*241-131C>A	ENSP00000505167.1:n.*241-131C>A
ENST00000681306.1:c.449-131C>A	ENSP00000506072.1:n.449-131C>A
ENST00000681618.1:c.326-131C>A	ENSP00000505773.1:n.326-131C>A
ENST00000681644.1:c.*121-131C>A	ENSP00000505180.1:n.*121-131C>A
ENST00000681806.1:c.449-131C>A	ENSP00000505282.1:n.449-131C>A
ENST00000382096.5:c.326-131C>A	ENSP00000371528.1:n.326-131C>A
ENST00000382099.2:c.449-131C>A	ENSP00000371531.2:n.449-131C>A
ENST00000382100.7:c.449-131C>A	ENSP00000371532.2:n.449-131C>A
NM_001018056.1:c.449-131C>A	NP_001018066.1:n.449-131C>A
NM_003383.3:c.449-131C>A	NP_003374.3:n.449-131C>A
XM_011518029.1:c.326-131C>A	XP_011516331.1:n.326-131C>A
NM_001018056.2:c.449-131C>A	NP_001018066.1:n.449-131C>A
NM_001322225.1:c.326-131C>A	NP_001309154.1:n.326-131C>A
NM_001322226.1:c.326-131C>A	NP_001309155.1:n.326-131C>A
NM_003383.4:c.449-131C>A	NP_003374.3:n.449-131C>A
XR_001746373.2:n.853-131C>A
XR_002956805.1:n.853-131C>A
NM_003383.5:c.449-131C>A MANE Select	NP_003374.3:n.449-131C>A
NM_001018056.3:c.449-131C>A	NP_001018066.1:n.449-131C>A
NM_001322225.2:c.326-131C>A	NP_001309154.1:n.326-131C>A
NM_001322226.2:c.326-131C>A	NP_001309155.1:n.326-131C>A