Canonical Allele Identifier: CA1828247991

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2650394T= , CM000671.2:g.2650394T=	GRCh38
NC_000009.11:g.2650394T= , CM000671.1:g.2650394T=	GRCh37
NC_000009.10:g.2640394T=	NCBI36
NG_012741.1:g.33602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1687T=
ENST00000382100.8:c.2129T= MANE Select	ENSP00000371532.2:p.Met710=
ENST00000679488.1:n.1555T=
ENST00000679718.1:n.1365T=
ENST00000679750.1:n.1545T=
ENST00000679780.1:n.905T=
ENST00000679851.1:n.2928T=
ENST00000680021.1:n.2329T=
ENST00000680043.1:c.1681T=
ENST00000680219.1:c.1696T=
ENST00000680243.1:c.*1768T=	ENSP00000505911.1:n.*1768T=
ENST00000680296.1:c.1555T=
ENST00000680332.1:n.1762T=
ENST00000680440.1:n.269T=
ENST00000680746.1:c.2006T=	ENSP00000505030.1:p.Met669=
ENST00000680751.1:n.1534T=
ENST00000680891.1:c.*1921T=	ENSP00000505167.1:n.*1921T=
ENST00000680975.1:n.1514T=
ENST00000681087.1:n.1434T=
ENST00000681306.1:c.2129T=	ENSP00000506072.1:p.Met710=
ENST00000681486.1:n.229T=
ENST00000681618.1:c.2006T=	ENSP00000505773.1:p.Met669=
ENST00000681644.1:c.*1801T=	ENSP00000505180.1:n.*1801T=
ENST00000681806.1:c.*567T=	ENSP00000505282.1:n.*567T=
ENST00000681942.1:c.1612T=
ENST00000382099.2:c.2129T=	ENSP00000371531.2:p.Met710=
ENST00000382100.7:c.2129T=	ENSP00000371532.2:p.Met710=
NM_001018056.1:c.2129T=	NP_001018066.1:p.Met710=
NM_003383.3:c.2129T=	NP_003374.3:p.Met710=
XM_011518029.1:c.2006T=	XP_011516331.1:p.Met669=
NM_001018056.2:c.2129T=	NP_001018066.1:p.Met710=
NM_001322225.1:c.2006T=	NP_001309154.1:p.Met669=
NM_001322226.1:c.2006T=	NP_001309155.1:p.Met669=
NM_003383.4:c.2129T=	NP_003374.3:p.Met710=
XR_001746373.2:n.2468T=
XR_002956805.1:n.2468T=
NM_003383.5:c.2129T= MANE Select	NP_003374.3:p.Met710=
NM_001018056.3:c.2129T=	NP_001018066.1:p.Met710=
NM_001322225.2:c.2006T=	NP_001309154.1:p.Met669=
NM_001322226.2:c.2006T=	NP_001309155.1:p.Met669=