Canonical Allele Identifier: CA372794544

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645667G>T (hg19) ; chr9:g.2645667G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645667G>T , CM000671.2:g.2645667G>T	GRCh38
NC_000009.11:g.2645667G>T , CM000671.1:g.2645667G>T	GRCh37
NC_000009.10:g.2635667G>T	NCBI36
NG_012741.1:g.28875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.964G>T
ENST00000382100.8:c.1406G>T MANE Select	ENSP00000371532.2:p.Arg469Ile
ENST00000478776.2:n.851G>T
ENST00000679718.1:n.642G>T
ENST00000679750.1:n.822G>T
ENST00000679851.1:n.1590G>T
ENST00000680021.1:n.1606G>T
ENST00000680043.1:c.958G>T
ENST00000680219.1:c.973G>T
ENST00000680243.1:c.*1185G>T	ENSP00000505911.1:n.*1185G>T
ENST00000680296.1:c.832G>T
ENST00000680332.1:n.489G>T
ENST00000680746.1:c.1283G>T	ENSP00000505030.1:p.Arg428Ile
ENST00000680751.1:n.811G>T
ENST00000680891.1:c.*1198G>T	ENSP00000505167.1:n.*1198G>T
ENST00000680975.1:n.791G>T
ENST00000681087.1:n.851G>T
ENST00000681306.1:c.1406G>T	ENSP00000506072.1:p.Arg469Ile
ENST00000681618.1:c.1283G>T	ENSP00000505773.1:p.Arg428Ile
ENST00000681644.1:c.*1078G>T	ENSP00000505180.1:n.*1078G>T
ENST00000681806.1:c.1406G>T	ENSP00000505282.1:p.Arg469Ile
ENST00000681942.1:c.954G>T
ENST00000382099.2:c.1406G>T	ENSP00000371531.2:p.Arg469Ile
ENST00000382100.7:c.1406G>T	ENSP00000371532.2:p.Arg469Ile
NM_001018056.1:c.1406G>T	NP_001018066.1:p.Arg469Ile
NM_003383.3:c.1406G>T	NP_003374.3:p.Arg469Ile
XM_011518029.1:c.1283G>T	XP_011516331.1:p.Arg428Ile
NM_001018056.2:c.1406G>T	NP_001018066.1:p.Arg469Ile
NM_001322225.1:c.1283G>T	NP_001309154.1:p.Arg428Ile
NM_001322226.1:c.1283G>T	NP_001309155.1:p.Arg428Ile
NM_003383.4:c.1406G>T	NP_003374.3:p.Arg469Ile
XR_001746373.2:n.1810G>T
XR_002956805.1:n.1810G>T
NM_003383.5:c.1406G>T MANE Select	NP_003374.3:p.Arg469Ile
NM_001018056.3:c.1406G>T	NP_001018066.1:p.Arg469Ile
NM_001322225.2:c.1283G>T	NP_001309154.1:p.Arg428Ile
NM_001322226.2:c.1283G>T	NP_001309155.1:p.Arg428Ile