Canonical Allele Identifier: CA463713055

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645608A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645608A>G , CM000671.2:g.2645608A>G	GRCh38
NC_000009.11:g.2645608A>G , CM000671.1:g.2645608A>G	GRCh37
NC_000009.10:g.2635608A>G	NCBI36
NG_012741.1:g.28816A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382099.3:c.905A>G
ENST00000382100.8:c.1347A>G MANE Select	ENSP00000371532.2:p.Arg449=
ENST00000478776.2:n.792A>G
ENST00000679718.1:n.583A>G
ENST00000679750.1:n.763A>G
ENST00000679851.1:n.1531A>G
ENST00000680021.1:n.1547A>G
ENST00000680043.1:c.899A>G
ENST00000680219.1:c.914A>G
ENST00000680243.1:c.*1126A>G	ENSP00000505911.1:n.*1126A>G
ENST00000680296.1:c.773A>G
ENST00000680332.1:n.430A>G
ENST00000680746.1:c.1224A>G	ENSP00000505030.1:p.Arg408=
ENST00000680751.1:n.752A>G
ENST00000680891.1:c.*1139A>G	ENSP00000505167.1:n.*1139A>G
ENST00000680975.1:n.732A>G
ENST00000681087.1:n.792A>G
ENST00000681306.1:c.1347A>G	ENSP00000506072.1:p.Arg449=
ENST00000681618.1:c.1224A>G	ENSP00000505773.1:p.Arg408=
ENST00000681644.1:c.*1019A>G	ENSP00000505180.1:n.*1019A>G
ENST00000681806.1:c.1347A>G	ENSP00000505282.1:p.Arg449=
ENST00000681942.1:c.895A>G
ENST00000382099.2:c.1347A>G	ENSP00000371531.2:p.Arg449=
ENST00000382100.7:c.1347A>G	ENSP00000371532.2:p.Arg449=
NM_001018056.1:c.1347A>G	NP_001018066.1:p.Arg449=
NM_003383.3:c.1347A>G	NP_003374.3:p.Arg449=
XM_011518029.1:c.1224A>G	XP_011516331.1:p.Arg408=
NM_001018056.2:c.1347A>G	NP_001018066.1:p.Arg449=
NM_001322225.1:c.1224A>G	NP_001309154.1:p.Arg408=
NM_001322226.1:c.1224A>G	NP_001309155.1:p.Arg408=
NM_003383.4:c.1347A>G	NP_003374.3:p.Arg449=
XR_001746373.2:n.1751A>G
XR_002956805.1:n.1751A>G
NM_003383.5:c.1347A>G MANE Select	NP_003374.3:p.Arg449=
NM_001018056.3:c.1347A>G	NP_001018066.1:p.Arg449=
NM_001322225.2:c.1224A>G	NP_001309154.1:p.Arg408=
NM_001322226.2:c.1224A>G	NP_001309155.1:p.Arg408=