Canonical Allele Identifier: CA1828247985

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2650382G= , CM000671.2:g.2650382G=	GRCh38
NC_000009.11:g.2650382G= , CM000671.1:g.2650382G=	GRCh37
NC_000009.10:g.2640382G=	NCBI36
NG_012741.1:g.33590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1675G=
ENST00000382100.8:c.2117G= MANE Select	ENSP00000371532.2:p.Cys706=
ENST00000679488.1:n.1543G=
ENST00000679718.1:n.1353G=
ENST00000679750.1:n.1533G=
ENST00000679780.1:n.893G=
ENST00000679851.1:n.2916G=
ENST00000680021.1:n.2317G=
ENST00000680043.1:c.1669G=
ENST00000680219.1:c.1684G=
ENST00000680243.1:c.*1756G=	ENSP00000505911.1:n.*1756G=
ENST00000680296.1:c.1543G=
ENST00000680332.1:n.1750G=
ENST00000680440.1:n.257G=
ENST00000680746.1:c.1994G=	ENSP00000505030.1:p.Cys665=
ENST00000680751.1:n.1522G=
ENST00000680891.1:c.*1909G=	ENSP00000505167.1:n.*1909G=
ENST00000680975.1:n.1502G=
ENST00000681087.1:n.1422G=
ENST00000681306.1:c.2117G=	ENSP00000506072.1:p.Cys706=
ENST00000681486.1:n.217G=
ENST00000681618.1:c.1994G=	ENSP00000505773.1:p.Cys665=
ENST00000681644.1:c.*1789G=	ENSP00000505180.1:n.*1789G=
ENST00000681806.1:c.*555G=	ENSP00000505282.1:n.*555G=
ENST00000681942.1:c.1600G=
ENST00000382099.2:c.2117G=	ENSP00000371531.2:p.Cys706=
ENST00000382100.7:c.2117G=	ENSP00000371532.2:p.Cys706=
NM_001018056.1:c.2117G=	NP_001018066.1:p.Cys706=
NM_003383.3:c.2117G=	NP_003374.3:p.Cys706=
XM_011518029.1:c.1994G=	XP_011516331.1:p.Cys665=
NM_001018056.2:c.2117G=	NP_001018066.1:p.Cys706=
NM_001322225.1:c.1994G=	NP_001309154.1:p.Cys665=
NM_001322226.1:c.1994G=	NP_001309155.1:p.Cys665=
NM_003383.4:c.2117G=	NP_003374.3:p.Cys706=
XR_001746373.2:n.2456G=
XR_002956805.1:n.2456G=
NM_003383.5:c.2117G= MANE Select	NP_003374.3:p.Cys706=
NM_001018056.3:c.2117G=	NP_001018066.1:p.Cys706=
NM_001322225.2:c.1994G=	NP_001309154.1:p.Cys665=
NM_001322226.2:c.1994G=	NP_001309155.1:p.Cys665=