Canonical Allele Identifier: CA1828244127

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643190C= , CM000671.2:g.2643190C=	GRCh38
NC_000009.11:g.2643190C= , CM000671.1:g.2643190C=	GRCh37
NC_000009.10:g.2633190C=	NCBI36
NG_012741.1:g.26398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.31C=
ENST00000382100.8:c.479C= MANE Select	ENSP00000371532.2:p.Thr160=
ENST00000679851.1:n.464C=
ENST00000680021.1:n.679C=
ENST00000680043.1:c.31C=
ENST00000680219.1:c.31C=
ENST00000680243.1:c.*258C=	ENSP00000505911.1:n.*258C=
ENST00000680296.1:c.31C=
ENST00000680746.1:c.356C=	ENSP00000505030.1:p.Thr119=
ENST00000680891.1:c.*271C=	ENSP00000505167.1:n.*271C=
ENST00000681306.1:c.479C=	ENSP00000506072.1:p.Thr160=
ENST00000681618.1:c.356C=	ENSP00000505773.1:p.Thr119=
ENST00000681644.1:c.*151C=	ENSP00000505180.1:n.*151C=
ENST00000681806.1:c.479C=	ENSP00000505282.1:p.Thr160=
ENST00000681942.1:c.31C=
ENST00000382096.5:c.356C=	ENSP00000371528.1:p.Thr119=
ENST00000382099.2:c.479C=	ENSP00000371531.2:p.Thr160=
ENST00000382100.7:c.479C=	ENSP00000371532.2:p.Thr160=
NM_001018056.1:c.479C=	NP_001018066.1:p.Thr160=
NM_003383.3:c.479C=	NP_003374.3:p.Thr160=
XM_011518029.1:c.356C=	XP_011516331.1:p.Thr119=
NM_001018056.2:c.479C=	NP_001018066.1:p.Thr160=
NM_001322225.1:c.356C=	NP_001309154.1:p.Thr119=
NM_001322226.1:c.356C=	NP_001309155.1:p.Thr119=
NM_003383.4:c.479C=	NP_003374.3:p.Thr160=
XR_001746373.2:n.883C=
XR_002956805.1:n.883C=
NM_003383.5:c.479C= MANE Select	NP_003374.3:p.Thr160=
NM_001018056.3:c.479C=	NP_001018066.1:p.Thr160=
NM_001322225.2:c.356C=	NP_001309154.1:p.Thr119=
NM_001322226.2:c.356C=	NP_001309155.1:p.Thr119=