Canonical Allele Identifier: CA1828246496

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647635_2647638delinsCATA , CM000671.2:g.2647635_2647638delinsCATA	GRCh38
NC_000009.11:g.2647635_2647638delinsCATA , CM000671.1:g.2647635_2647638delinsCATA	GRCh37
NC_000009.10:g.2637635_2637638delinsCATA	NCBI36
NG_012741.1:g.30843_30846delinsCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+43_1380+46delinsCATA
ENST00000382100.8:c.1822+43_1822+46delinsCATA MANE Select	ENSP00000371532.2:n.1822+43_1822+46delinsCATA
ENST00000478776.2:n.1310_1313delinsCATA
ENST00000679488.1:n.355_358delinsCATA
ENST00000679718.1:n.1058+43_1058+46delinsCATA
ENST00000679750.1:n.1238+43_1238+46delinsCATA
ENST00000679780.1:n.26_29delinsCATA
ENST00000679851.1:n.2049_2052delinsCATA
ENST00000680021.1:n.2022+43_2022+46delinsCATA
ENST00000680043.1:c.1374+43_1374+46delinsCATA
ENST00000680219.1:c.1389+43_1389+46delinsCATA
ENST00000680243.1:c.*1601+43_*1601+46delinsCATA	ENSP00000505911.1:n.*1601+43_*1601+46delinsCATA
ENST00000680296.1:c.1248+43_1248+46delinsCATA
ENST00000680332.1:n.883_886delinsCATA
ENST00000680746.1:c.1699+43_1699+46delinsCATA	ENSP00000505030.1:n.1699+43_1699+46delinsCATA
ENST00000680751.1:n.1227+43_1227+46delinsCATA
ENST00000680891.1:c.*1614+43_*1614+46delinsCATA	ENSP00000505167.1:n.*1614+43_*1614+46delinsCATA
ENST00000680975.1:n.1207+43_1207+46delinsCATA
ENST00000681087.1:n.1267+43_1267+46delinsCATA
ENST00000681306.1:c.1822+43_1822+46delinsCATA	ENSP00000506072.1:n.1822+43_1822+46delinsCATA
ENST00000681618.1:c.1699+43_1699+46delinsCATA	ENSP00000505773.1:n.1699+43_1699+46delinsCATA
ENST00000681644.1:c.*1494+43_*1494+46delinsCATA	ENSP00000505180.1:n.*1494+43_*1494+46delinsCATA
ENST00000681806.1:c.*260+43_*260+46delinsCATA	ENSP00000505282.1:n.*260+43_*260+46delinsCATA
ENST00000681942.1:c.1305+43_1305+46delinsCATA
ENST00000382099.2:c.1822+43_1822+46delinsCATA	ENSP00000371531.2:n.1822+43_1822+46delinsCATA
ENST00000382100.7:c.1822+43_1822+46delinsCATA	ENSP00000371532.2:n.1822+43_1822+46delinsCATA
ENST00000478776.1:n.377_380delinsCATA
NM_001018056.1:c.1822+43_1822+46delinsCATA	NP_001018066.1:n.1822+43_1822+46delinsCATA
NM_003383.3:c.1822+43_1822+46delinsCATA	NP_003374.3:n.1822+43_1822+46delinsCATA
XM_011518029.1:c.1699+43_1699+46delinsCATA	XP_011516331.1:n.1699+43_1699+46delinsCATA
NM_001018056.2:c.1822+43_1822+46delinsCATA	NP_001018066.1:n.1822+43_1822+46delinsCATA
NM_001322225.1:c.1699+43_1699+46delinsCATA	NP_001309154.1:n.1699+43_1699+46delinsCATA
NM_001322226.1:c.1699+43_1699+46delinsCATA	NP_001309155.1:n.1699+43_1699+46delinsCATA
NM_003383.4:c.1822+43_1822+46delinsCATA	NP_003374.3:n.1822+43_1822+46delinsCATA
XR_001746373.2:n.2161+43_2161+46delinsCATA
XR_002956805.1:n.2161+43_2161+46delinsCATA
NM_003383.5:c.1822+43_1822+46delinsCATA MANE Select	NP_003374.3:n.1822+43_1822+46delinsCATA
NM_001018056.3:c.1822+43_1822+46delinsCATA	NP_001018066.1:n.1822+43_1822+46delinsCATA
NM_001322225.2:c.1699+43_1699+46delinsCATA	NP_001309154.1:n.1699+43_1699+46delinsCATA
NM_001322226.2:c.1699+43_1699+46delinsCATA	NP_001309155.1:n.1699+43_1699+46delinsCATA