Canonical Allele Identifier: CA1828246516

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647682_2647684delinsACT , CM000671.2:g.2647682_2647684delinsACT	GRCh38
NC_000009.11:g.2647682_2647684delinsACT , CM000671.1:g.2647682_2647684delinsACT	GRCh37
NC_000009.10:g.2637682_2637684delinsACT	NCBI36
NG_012741.1:g.30890_30892delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+90_1380+92delinsACT
ENST00000382100.8:c.1822+90_1822+92delinsACT MANE Select	ENSP00000371532.2:n.1822+90_1822+92delinsACT
ENST00000478776.2:n.1357_1359delinsACT
ENST00000679488.1:n.402_404delinsACT
ENST00000679718.1:n.1058+90_1058+92delinsACT
ENST00000679750.1:n.1238+90_1238+92delinsACT
ENST00000679780.1:n.73_75delinsACT
ENST00000679851.1:n.2096_2098delinsACT
ENST00000680021.1:n.2022+90_2022+92delinsACT
ENST00000680043.1:c.1374+90_1374+92delinsACT
ENST00000680219.1:c.1389+90_1389+92delinsACT
ENST00000680243.1:c.*1601+90_*1601+92delinsACT	ENSP00000505911.1:n.*1601+90_*1601+92delinsACT
ENST00000680296.1:c.1248+90_1248+92delinsACT
ENST00000680332.1:n.930_932delinsACT
ENST00000680746.1:c.1699+90_1699+92delinsACT	ENSP00000505030.1:n.1699+90_1699+92delinsACT
ENST00000680751.1:n.1227+90_1227+92delinsACT
ENST00000680891.1:c.*1614+90_*1614+92delinsACT	ENSP00000505167.1:n.*1614+90_*1614+92delinsACT
ENST00000680975.1:n.1207+90_1207+92delinsACT
ENST00000681087.1:n.1267+90_1267+92delinsACT
ENST00000681306.1:c.1822+90_1822+92delinsACT	ENSP00000506072.1:n.1822+90_1822+92delinsACT
ENST00000681618.1:c.1699+90_1699+92delinsACT	ENSP00000505773.1:n.1699+90_1699+92delinsACT
ENST00000681644.1:c.*1494+90_*1494+92delinsACT	ENSP00000505180.1:n.*1494+90_*1494+92delinsACT
ENST00000681806.1:c.*260+90_*260+92delinsACT	ENSP00000505282.1:n.*260+90_*260+92delinsACT
ENST00000681942.1:c.1305+90_1305+92delinsACT
ENST00000382099.2:c.1822+90_1822+92delinsACT	ENSP00000371531.2:n.1822+90_1822+92delinsACT
ENST00000382100.7:c.1822+90_1822+92delinsACT	ENSP00000371532.2:n.1822+90_1822+92delinsACT
ENST00000478776.1:n.424_426delinsACT
NM_001018056.1:c.1822+90_1822+92delinsACT	NP_001018066.1:n.1822+90_1822+92delinsACT
NM_003383.3:c.1822+90_1822+92delinsACT	NP_003374.3:n.1822+90_1822+92delinsACT
XM_011518029.1:c.1699+90_1699+92delinsACT	XP_011516331.1:n.1699+90_1699+92delinsACT
NM_001018056.2:c.1822+90_1822+92delinsACT	NP_001018066.1:n.1822+90_1822+92delinsACT
NM_001322225.1:c.1699+90_1699+92delinsACT	NP_001309154.1:n.1699+90_1699+92delinsACT
NM_001322226.1:c.1699+90_1699+92delinsACT	NP_001309155.1:n.1699+90_1699+92delinsACT
NM_003383.4:c.1822+90_1822+92delinsACT	NP_003374.3:n.1822+90_1822+92delinsACT
XR_001746373.2:n.2161+90_2161+92delinsACT
XR_002956805.1:n.2161+90_2161+92delinsACT
NM_003383.5:c.1822+90_1822+92delinsACT MANE Select	NP_003374.3:n.1822+90_1822+92delinsACT
NM_001018056.3:c.1822+90_1822+92delinsACT	NP_001018066.1:n.1822+90_1822+92delinsACT
NM_001322225.2:c.1699+90_1699+92delinsACT	NP_001309154.1:n.1699+90_1699+92delinsACT
NM_001322226.2:c.1699+90_1699+92delinsACT	NP_001309155.1:n.1699+90_1699+92delinsACT