Canonical Allele Identifier: CA1828245496

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645633_2645634delinsAG , CM000671.2:g.2645633_2645634delinsAG	GRCh38
NC_000009.11:g.2645633_2645634delinsAG , CM000671.1:g.2645633_2645634delinsAG	GRCh37
NC_000009.10:g.2635633_2635634delinsAG	NCBI36
NG_012741.1:g.28841_28842delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.930_931delinsAG
ENST00000382100.8:c.1372_1373delinsAG MANE Select	ENSP00000371532.2:p.Arg458=
ENST00000478776.2:n.817_818delinsAG
ENST00000679718.1:n.608_609delinsAG
ENST00000679750.1:n.788_789delinsAG
ENST00000679851.1:n.1556_1557delinsAG
ENST00000680021.1:n.1572_1573delinsAG
ENST00000680043.1:c.924_925delinsAG
ENST00000680219.1:c.939_940delinsAG
ENST00000680243.1:c.*1151_*1152delinsAG	ENSP00000505911.1:n.*1151_*1152delinsAG
ENST00000680296.1:c.798_799delinsAG
ENST00000680332.1:n.455_456delinsAG
ENST00000680746.1:c.1249_1250delinsAG	ENSP00000505030.1:p.Arg417=
ENST00000680751.1:n.777_778delinsAG
ENST00000680891.1:c.*1164_*1165delinsAG	ENSP00000505167.1:n.*1164_*1165delinsAG
ENST00000680975.1:n.757_758delinsAG
ENST00000681087.1:n.817_818delinsAG
ENST00000681306.1:c.1372_1373delinsAG	ENSP00000506072.1:p.Arg458=
ENST00000681618.1:c.1249_1250delinsAG	ENSP00000505773.1:p.Arg417=
ENST00000681644.1:c.*1044_*1045delinsAG	ENSP00000505180.1:n.*1044_*1045delinsAG
ENST00000681806.1:c.1372_1373delinsAG	ENSP00000505282.1:p.Arg458=
ENST00000681942.1:c.920_921delinsAG
ENST00000382099.2:c.1372_1373delinsAG	ENSP00000371531.2:p.Arg458=
ENST00000382100.7:c.1372_1373delinsAG	ENSP00000371532.2:p.Arg458=
NM_001018056.1:c.1372_1373delinsAG	NP_001018066.1:p.Arg458=
NM_003383.3:c.1372_1373delinsAG	NP_003374.3:p.Arg458=
XM_011518029.1:c.1249_1250delinsAG	XP_011516331.1:p.Arg417=
NM_001018056.2:c.1372_1373delinsAG	NP_001018066.1:p.Arg458=
NM_001322225.1:c.1249_1250delinsAG	NP_001309154.1:p.Arg417=
NM_001322226.1:c.1249_1250delinsAG	NP_001309155.1:p.Arg417=
NM_003383.4:c.1372_1373delinsAG	NP_003374.3:p.Arg458=
XR_001746373.2:n.1776_1777delinsAG
XR_002956805.1:n.1776_1777delinsAG
NM_003383.5:c.1372_1373delinsAG MANE Select	NP_003374.3:p.Arg458=
NM_001018056.3:c.1372_1373delinsAG	NP_001018066.1:p.Arg458=
NM_001322225.2:c.1249_1250delinsAG	NP_001309154.1:p.Arg417=
NM_001322226.2:c.1249_1250delinsAG	NP_001309155.1:p.Arg417=