Canonical Allele Identifier: CA2579302268

Gene: VLDLR

Linked Data

• gnomAD v4: 9-2647599-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647599A>G , CM000671.2:g.2647599A>G	GRCh38
NC_000009.11:g.2647599A>G , CM000671.1:g.2647599A>G	GRCh37
NC_000009.10:g.2637599A>G	NCBI36
NG_012741.1:g.30807A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+7A>G
ENST00000382100.8:c.1822+7A>G MANE Select	ENSP00000371532.2:n.1822+7A>G
ENST00000478776.2:n.1274A>G
ENST00000679488.1:n.319A>G
ENST00000679718.1:n.1058+7A>G
ENST00000679750.1:n.1238+7A>G
ENST00000679851.1:n.2013A>G
ENST00000680021.1:n.2022+7A>G
ENST00000680043.1:c.1374+7A>G
ENST00000680219.1:c.1389+7A>G
ENST00000680243.1:c.*1601+7A>G	ENSP00000505911.1:n.*1601+7A>G
ENST00000680296.1:c.1248+7A>G
ENST00000680332.1:n.847A>G
ENST00000680746.1:c.1699+7A>G	ENSP00000505030.1:n.1699+7A>G
ENST00000680751.1:n.1227+7A>G
ENST00000680891.1:c.*1614+7A>G	ENSP00000505167.1:n.*1614+7A>G
ENST00000680975.1:n.1207+7A>G
ENST00000681087.1:n.1267+7A>G
ENST00000681306.1:c.1822+7A>G	ENSP00000506072.1:n.1822+7A>G
ENST00000681618.1:c.1699+7A>G	ENSP00000505773.1:n.1699+7A>G
ENST00000681644.1:c.*1494+7A>G	ENSP00000505180.1:n.*1494+7A>G
ENST00000681806.1:c.*260+7A>G	ENSP00000505282.1:n.*260+7A>G
ENST00000681942.1:c.1305+7A>G
ENST00000382099.2:c.1822+7A>G	ENSP00000371531.2:n.1822+7A>G
ENST00000382100.7:c.1822+7A>G	ENSP00000371532.2:n.1822+7A>G
ENST00000478776.1:n.341A>G
NM_001018056.1:c.1822+7A>G	NP_001018066.1:n.1822+7A>G
NM_003383.3:c.1822+7A>G	NP_003374.3:n.1822+7A>G
XM_011518029.1:c.1699+7A>G	XP_011516331.1:n.1699+7A>G
NM_001018056.2:c.1822+7A>G	NP_001018066.1:n.1822+7A>G
NM_001322225.1:c.1699+7A>G	NP_001309154.1:n.1699+7A>G
NM_001322226.1:c.1699+7A>G	NP_001309155.1:n.1699+7A>G
NM_003383.4:c.1822+7A>G	NP_003374.3:n.1822+7A>G
XR_001746373.2:n.2161+7A>G
XR_002956805.1:n.2161+7A>G
NM_003383.5:c.1822+7A>G MANE Select	NP_003374.3:n.1822+7A>G
NM_001018056.3:c.1822+7A>G	NP_001018066.1:n.1822+7A>G
NM_001322225.2:c.1699+7A>G	NP_001309154.1:n.1699+7A>G
NM_001322226.2:c.1699+7A>G	NP_001309155.1:n.1699+7A>G