Canonical Allele Identifier: CA463852780

Gene: VLDLR

Linked Data

• gnomAD v4: 9-2643164-T-C
• MyVariant Identifiers: chr9:g.2643164T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643164T>C , CM000671.2:g.2643164T>C	GRCh38
NC_000009.11:g.2643164T>C , CM000671.1:g.2643164T>C	GRCh37
NC_000009.10:g.2633164T>C	NCBI36
NG_012741.1:g.26372T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.5T>C
ENST00000382100.8:c.453T>C MANE Select	ENSP00000371532.2:p.Asn151=
ENST00000679851.1:n.438T>C
ENST00000680021.1:n.653T>C
ENST00000680043.1:c.5T>C
ENST00000680219.1:c.5T>C
ENST00000680243.1:c.*232T>C	ENSP00000505911.1:n.*232T>C
ENST00000680296.1:c.5T>C
ENST00000680746.1:c.330T>C	ENSP00000505030.1:p.Asn110=
ENST00000680891.1:c.*245T>C	ENSP00000505167.1:n.*245T>C
ENST00000681306.1:c.453T>C	ENSP00000506072.1:p.Asn151=
ENST00000681618.1:c.330T>C	ENSP00000505773.1:p.Asn110=
ENST00000681644.1:c.*125T>C	ENSP00000505180.1:n.*125T>C
ENST00000681806.1:c.453T>C	ENSP00000505282.1:p.Asn151=
ENST00000681942.1:c.5T>C
ENST00000382096.5:c.330T>C	ENSP00000371528.1:p.Asn110=
ENST00000382099.2:c.453T>C	ENSP00000371531.2:p.Asn151=
ENST00000382100.7:c.453T>C	ENSP00000371532.2:p.Asn151=
NM_001018056.1:c.453T>C	NP_001018066.1:p.Asn151=
NM_003383.3:c.453T>C	NP_003374.3:p.Asn151=
XM_011518029.1:c.330T>C	XP_011516331.1:p.Asn110=
NM_001018056.2:c.453T>C	NP_001018066.1:p.Asn151=
NM_001322225.1:c.330T>C	NP_001309154.1:p.Asn110=
NM_001322226.1:c.330T>C	NP_001309155.1:p.Asn110=
NM_003383.4:c.453T>C	NP_003374.3:p.Asn151=
XR_001746373.2:n.857T>C
XR_002956805.1:n.857T>C
NM_003383.5:c.453T>C MANE Select	NP_003374.3:p.Asn151=
NM_001018056.3:c.453T>C	NP_001018066.1:p.Asn151=
NM_001322225.2:c.330T>C	NP_001309154.1:p.Asn110=
NM_001322226.2:c.330T>C	NP_001309155.1:p.Asn110=