Canonical Allele Identifier: CA372793377

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2644743A>T (hg19) ; chr9:g.2644743A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2644743A>T , CM000671.2:g.2644743A>T	GRCh38
NC_000009.11:g.2644743A>T , CM000671.1:g.2644743A>T	GRCh37
NC_000009.10:g.2634743A>T	NCBI36
NG_012741.1:g.27951A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382099.3:c.634A>T
ENST00000382100.8:c.1076A>T MANE Select	ENSP00000371532.2:p.Glu359Val
ENST00000478776.2:n.418A>T
ENST00000679718.1:n.209A>T
ENST00000679750.1:n.389A>T
ENST00000679851.1:n.1157A>T
ENST00000680021.1:n.1276A>T
ENST00000680043.1:c.628A>T
ENST00000680150.1:n.256A>T
ENST00000680219.1:c.628A>T
ENST00000680243.1:c.*855A>T	ENSP00000505911.1:n.*855A>T
ENST00000680296.1:c.628A>T
ENST00000680332.1:n.56A>T
ENST00000680746.1:c.953A>T	ENSP00000505030.1:p.Glu318Val
ENST00000680751.1:n.378A>T
ENST00000680891.1:c.*868A>T	ENSP00000505167.1:n.*868A>T
ENST00000680975.1:n.358A>T
ENST00000681087.1:n.418A>T
ENST00000681306.1:c.1076A>T	ENSP00000506072.1:p.Glu359Val
ENST00000681618.1:c.953A>T	ENSP00000505773.1:p.Glu318Val
ENST00000681644.1:c.*748A>T	ENSP00000505180.1:n.*748A>T
ENST00000681806.1:c.1076A>T	ENSP00000505282.1:p.Glu359Val
ENST00000681942.1:c.628A>T
ENST00000382099.2:c.1076A>T	ENSP00000371531.2:p.Glu359Val
ENST00000382100.7:c.1076A>T	ENSP00000371532.2:p.Glu359Val
NM_001018056.1:c.1076A>T	NP_001018066.1:p.Glu359Val
NM_003383.3:c.1076A>T	NP_003374.3:p.Glu359Val
XM_011518029.1:c.953A>T	XP_011516331.1:p.Glu318Val
NM_001018056.2:c.1076A>T	NP_001018066.1:p.Glu359Val
NM_001322225.1:c.953A>T	NP_001309154.1:p.Glu318Val
NM_001322226.1:c.953A>T	NP_001309155.1:p.Glu318Val
NM_003383.4:c.1076A>T	NP_003374.3:p.Glu359Val
XR_001746373.2:n.1480A>T
XR_002956805.1:n.1480A>T
NM_003383.5:c.1076A>T MANE Select	NP_003374.3:p.Glu359Val
NM_001018056.3:c.1076A>T	NP_001018066.1:p.Glu359Val
NM_001322225.2:c.953A>T	NP_001309154.1:p.Glu318Val
NM_001322226.2:c.953A>T	NP_001309155.1:p.Glu318Val