Canonical Allele Identifier: CA463713075

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645651C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645651C>T , CM000671.2:g.2645651C>T	GRCh38
NC_000009.11:g.2645651C>T , CM000671.1:g.2645651C>T	GRCh37
NC_000009.10:g.2635651C>T	NCBI36
NG_012741.1:g.28859C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.948C>T
ENST00000382100.8:c.1390C>T MANE Select	ENSP00000371532.2:p.Leu464=
ENST00000478776.2:n.835C>T
ENST00000679718.1:n.626C>T
ENST00000679750.1:n.806C>T
ENST00000679851.1:n.1574C>T
ENST00000680021.1:n.1590C>T
ENST00000680043.1:c.942C>T
ENST00000680219.1:c.957C>T
ENST00000680243.1:c.*1169C>T	ENSP00000505911.1:n.*1169C>T
ENST00000680296.1:c.816C>T
ENST00000680332.1:n.473C>T
ENST00000680746.1:c.1267C>T	ENSP00000505030.1:p.Leu423=
ENST00000680751.1:n.795C>T
ENST00000680891.1:c.*1182C>T	ENSP00000505167.1:n.*1182C>T
ENST00000680975.1:n.775C>T
ENST00000681087.1:n.835C>T
ENST00000681306.1:c.1390C>T	ENSP00000506072.1:p.Leu464=
ENST00000681618.1:c.1267C>T	ENSP00000505773.1:p.Leu423=
ENST00000681644.1:c.*1062C>T	ENSP00000505180.1:n.*1062C>T
ENST00000681806.1:c.1390C>T	ENSP00000505282.1:p.Leu464=
ENST00000681942.1:c.938C>T
ENST00000382099.2:c.1390C>T	ENSP00000371531.2:p.Leu464=
ENST00000382100.7:c.1390C>T	ENSP00000371532.2:p.Leu464=
NM_001018056.1:c.1390C>T	NP_001018066.1:p.Leu464=
NM_003383.3:c.1390C>T	NP_003374.3:p.Leu464=
XM_011518029.1:c.1267C>T	XP_011516331.1:p.Leu423=
NM_001018056.2:c.1390C>T	NP_001018066.1:p.Leu464=
NM_001322225.1:c.1267C>T	NP_001309154.1:p.Leu423=
NM_001322226.1:c.1267C>T	NP_001309155.1:p.Leu423=
NM_003383.4:c.1390C>T	NP_003374.3:p.Leu464=
XR_001746373.2:n.1794C>T
XR_002956805.1:n.1794C>T
NM_003383.5:c.1390C>T MANE Select	NP_003374.3:p.Leu464=
NM_001018056.3:c.1390C>T	NP_001018066.1:p.Leu464=
NM_001322225.2:c.1267C>T	NP_001309154.1:p.Leu423=
NM_001322226.2:c.1267C>T	NP_001309155.1:p.Leu423=