Canonical Allele Identifier: CA1828244091

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643121C= , CM000671.2:g.2643121C=	GRCh38
NC_000009.11:g.2643121C= , CM000671.1:g.2643121C=	GRCh37
NC_000009.10:g.2633121C=	NCBI36
NG_012741.1:g.26329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382100.8:c.449-39C= MANE Select	ENSP00000371532.2:n.449-39C=
ENST00000679851.1:n.434-39C=
ENST00000680021.1:n.649-39C=
ENST00000680243.1:c.*228-39C=	ENSP00000505911.1:n.*228-39C=
ENST00000680746.1:c.326-39C=	ENSP00000505030.1:n.326-39C=
ENST00000680891.1:c.*241-39C=	ENSP00000505167.1:n.*241-39C=
ENST00000681306.1:c.449-39C=	ENSP00000506072.1:n.449-39C=
ENST00000681618.1:c.326-39C=	ENSP00000505773.1:n.326-39C=
ENST00000681644.1:c.*121-39C=	ENSP00000505180.1:n.*121-39C=
ENST00000681806.1:c.449-39C=	ENSP00000505282.1:n.449-39C=
ENST00000382096.5:c.326-39C=	ENSP00000371528.1:n.326-39C=
ENST00000382099.2:c.449-39C=	ENSP00000371531.2:n.449-39C=
ENST00000382100.7:c.449-39C=	ENSP00000371532.2:n.449-39C=
NM_001018056.1:c.449-39C=	NP_001018066.1:n.449-39C=
NM_003383.3:c.449-39C=	NP_003374.3:n.449-39C=
XM_011518029.1:c.326-39C=	XP_011516331.1:n.326-39C=
NM_001018056.2:c.449-39C=	NP_001018066.1:n.449-39C=
NM_001322225.1:c.326-39C=	NP_001309154.1:n.326-39C=
NM_001322226.1:c.326-39C=	NP_001309155.1:n.326-39C=
NM_003383.4:c.449-39C=	NP_003374.3:n.449-39C=
XR_001746373.2:n.853-39C=
XR_002956805.1:n.853-39C=
NM_003383.5:c.449-39C= MANE Select	NP_003374.3:n.449-39C=
NM_001018056.3:c.449-39C=	NP_001018066.1:n.449-39C=
NM_001322225.2:c.326-39C=	NP_001309154.1:n.326-39C=
NM_001322226.2:c.326-39C=	NP_001309155.1:n.326-39C=