Canonical Allele Identifier: CA918397076

Gene: VLDLR

Linked Data

• dbSNP Id: rs1586655702
• gnomAD v3: 9-2647649-T-TTA
• gnomAD v4: 9-2647649-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647651_2647652dup , CM000671.2:g.2647651_2647652dup	GRCh38
NC_000009.11:g.2647651_2647652dup , CM000671.1:g.2647651_2647652dup	GRCh37
NC_000009.10:g.2637651_2637652dup	NCBI36
NG_012741.1:g.30859_30860dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+59_1380+60dup
ENST00000382100.8:c.1822+59_1822+60dup MANE Select	ENSP00000371532.2:n.1822+59_1822+60dup
ENST00000478776.2:n.1326_1327dup
ENST00000679488.1:n.371_372dup
ENST00000679718.1:n.1058+59_1058+60dup
ENST00000679750.1:n.1238+59_1238+60dup
ENST00000679780.1:n.42_43dup
ENST00000679851.1:n.2065_2066dup
ENST00000680021.1:n.2022+59_2022+60dup
ENST00000680043.1:c.1374+59_1374+60dup
ENST00000680219.1:c.1389+59_1389+60dup
ENST00000680243.1:c.*1601+59_*1601+60dup	ENSP00000505911.1:n.*1601+59_*1601+60dup
ENST00000680296.1:c.1248+59_1248+60dup
ENST00000680332.1:n.899_900dup
ENST00000680746.1:c.1699+59_1699+60dup	ENSP00000505030.1:n.1699+59_1699+60dup
ENST00000680751.1:n.1227+59_1227+60dup
ENST00000680891.1:c.*1614+59_*1614+60dup	ENSP00000505167.1:n.*1614+59_*1614+60dup
ENST00000680975.1:n.1207+59_1207+60dup
ENST00000681087.1:n.1267+59_1267+60dup
ENST00000681306.1:c.1822+59_1822+60dup	ENSP00000506072.1:n.1822+59_1822+60dup
ENST00000681618.1:c.1699+59_1699+60dup	ENSP00000505773.1:n.1699+59_1699+60dup
ENST00000681644.1:c.*1494+59_*1494+60dup	ENSP00000505180.1:n.*1494+59_*1494+60dup
ENST00000681806.1:c.*260+59_*260+60dup	ENSP00000505282.1:n.*260+59_*260+60dup
ENST00000681942.1:c.1305+59_1305+60dup
ENST00000382099.2:c.1822+59_1822+60dup	ENSP00000371531.2:n.1822+59_1822+60dup
ENST00000382100.7:c.1822+59_1822+60dup	ENSP00000371532.2:n.1822+59_1822+60dup
ENST00000478776.1:n.393_394dup
NM_001018056.1:c.1822+59_1822+60dup	NP_001018066.1:n.1822+59_1822+60dup
NM_003383.3:c.1822+59_1822+60dup	NP_003374.3:n.1822+59_1822+60dup
XM_011518029.1:c.1699+59_1699+60dup	XP_011516331.1:n.1699+59_1699+60dup
NM_001018056.2:c.1822+59_1822+60dup	NP_001018066.1:n.1822+59_1822+60dup
NM_001322225.1:c.1699+59_1699+60dup	NP_001309154.1:n.1699+59_1699+60dup
NM_001322226.1:c.1699+59_1699+60dup	NP_001309155.1:n.1699+59_1699+60dup
NM_003383.4:c.1822+59_1822+60dup	NP_003374.3:n.1822+59_1822+60dup
XR_001746373.2:n.2161+59_2161+60dup
XR_002956805.1:n.2161+59_2161+60dup
NM_003383.5:c.1822+59_1822+60dup MANE Select	NP_003374.3:n.1822+59_1822+60dup
NM_001018056.3:c.1822+59_1822+60dup	NP_001018066.1:n.1822+59_1822+60dup
NM_001322225.2:c.1699+59_1699+60dup	NP_001309154.1:n.1699+59_1699+60dup
NM_001322226.2:c.1699+59_1699+60dup	NP_001309155.1:n.1699+59_1699+60dup