Canonical Allele Identifier: CA1828245627

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645918T= , CM000671.2:g.2645918T=	GRCh38
NC_000009.11:g.2645918T= , CM000671.1:g.2645918T=	GRCh37
NC_000009.10:g.2635918T=	NCBI36
NG_012741.1:g.29126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1042+173T=
ENST00000382100.8:c.1484+173T= MANE Select	ENSP00000371532.2:n.1484+173T=
ENST00000478776.2:n.929+173T=
ENST00000679718.1:n.720+173T=
ENST00000679750.1:n.900+173T=
ENST00000679851.1:n.1668+173T=
ENST00000680021.1:n.1684+173T=
ENST00000680043.1:c.1036+173T=
ENST00000680219.1:c.1051+173T=
ENST00000680243.1:c.*1263+173T=	ENSP00000505911.1:n.*1263+173T=
ENST00000680296.1:c.910+173T=
ENST00000680332.1:n.567+173T=
ENST00000680746.1:c.1361+173T=	ENSP00000505030.1:n.1361+173T=
ENST00000680751.1:n.889+173T=
ENST00000680891.1:c.*1276+173T=	ENSP00000505167.1:n.*1276+173T=
ENST00000680975.1:n.869+173T=
ENST00000681087.1:n.929+173T=
ENST00000681306.1:c.1484+173T=	ENSP00000506072.1:n.1484+173T=
ENST00000681618.1:c.1361+173T=	ENSP00000505773.1:n.1361+173T=
ENST00000681644.1:c.*1156+173T=	ENSP00000505180.1:n.*1156+173T=
ENST00000681806.1:c.1484+173T=	ENSP00000505282.1:n.1484+173T=
ENST00000681942.1:c.1032+173T=
ENST00000382099.2:c.1484+173T=	ENSP00000371531.2:n.1484+173T=
ENST00000382100.7:c.1484+173T=	ENSP00000371532.2:n.1484+173T=
NM_001018056.1:c.1484+173T=	NP_001018066.1:n.1484+173T=
NM_003383.3:c.1484+173T=	NP_003374.3:n.1484+173T=
XM_011518029.1:c.1361+173T=	XP_011516331.1:n.1361+173T=
NM_001018056.2:c.1484+173T=	NP_001018066.1:n.1484+173T=
NM_001322225.1:c.1361+173T=	NP_001309154.1:n.1361+173T=
NM_001322226.1:c.1361+173T=	NP_001309155.1:n.1361+173T=
NM_003383.4:c.1484+173T=	NP_003374.3:n.1484+173T=
XR_001746373.2:n.1888+173T=
XR_002956805.1:n.1888+173T=
NM_003383.5:c.1484+173T= MANE Select	NP_003374.3:n.1484+173T=
NM_001018056.3:c.1484+173T=	NP_001018066.1:n.1484+173T=
NM_001322225.2:c.1361+173T=	NP_001309154.1:n.1361+173T=
NM_001322226.2:c.1361+173T=	NP_001309155.1:n.1361+173T=