Canonical Allele Identifier: CA1828245475

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645590G= , CM000671.2:g.2645590G=	GRCh38
NC_000009.11:g.2645590G= , CM000671.1:g.2645590G=	GRCh37
NC_000009.10:g.2635590G=	NCBI36
NG_012741.1:g.28798G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.887G=
ENST00000382100.8:c.1329G= MANE Select	ENSP00000371532.2:p.Leu443=
ENST00000478776.2:n.774G=
ENST00000679718.1:n.565G=
ENST00000679750.1:n.745G=
ENST00000679851.1:n.1513G=
ENST00000680021.1:n.1529G=
ENST00000680043.1:c.881G=
ENST00000680219.1:c.896G=
ENST00000680243.1:c.*1108G=	ENSP00000505911.1:n.*1108G=
ENST00000680296.1:c.755G=
ENST00000680332.1:n.412G=
ENST00000680746.1:c.1206G=	ENSP00000505030.1:p.Leu402=
ENST00000680751.1:n.734G=
ENST00000680891.1:c.*1121G=	ENSP00000505167.1:n.*1121G=
ENST00000680975.1:n.714G=
ENST00000681087.1:n.774G=
ENST00000681306.1:c.1329G=	ENSP00000506072.1:p.Leu443=
ENST00000681618.1:c.1206G=	ENSP00000505773.1:p.Leu402=
ENST00000681644.1:c.*1001G=	ENSP00000505180.1:n.*1001G=
ENST00000681806.1:c.1329G=	ENSP00000505282.1:p.Leu443=
ENST00000681942.1:c.877G=
ENST00000382099.2:c.1329G=	ENSP00000371531.2:p.Leu443=
ENST00000382100.7:c.1329G=	ENSP00000371532.2:p.Leu443=
NM_001018056.1:c.1329G=	NP_001018066.1:p.Leu443=
NM_003383.3:c.1329G=	NP_003374.3:p.Leu443=
XM_011518029.1:c.1206G=	XP_011516331.1:p.Leu402=
NM_001018056.2:c.1329G=	NP_001018066.1:p.Leu443=
NM_001322225.1:c.1206G=	NP_001309154.1:p.Leu402=
NM_001322226.1:c.1206G=	NP_001309155.1:p.Leu402=
NM_003383.4:c.1329G=	NP_003374.3:p.Leu443=
XR_001746373.2:n.1733G=
XR_002956805.1:n.1733G=
NM_003383.5:c.1329G= MANE Select	NP_003374.3:p.Leu443=
NM_001018056.3:c.1329G=	NP_001018066.1:p.Leu443=
NM_001322225.2:c.1206G=	NP_001309154.1:p.Leu402=
NM_001322226.2:c.1206G=	NP_001309155.1:p.Leu402=