Canonical Allele Identifier: CA862632184

Gene: VLDLR

Linked Data

• dbSNP Id: rs1489059032
• gnomAD v4: 9-2647682-ACT-A
• MyVariant Identifiers: chr9:g.2647683_2647684del (hg19) ; chr9:g.2647683_2647684del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647685_2647686del , CM000671.2:g.2647685_2647686del	GRCh38
NC_000009.11:g.2647685_2647686del , CM000671.1:g.2647685_2647686del	GRCh37
NC_000009.10:g.2637685_2637686del	NCBI36
NG_012741.1:g.30893_30894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+93_1380+94del
ENST00000382100.8:c.1822+93_1822+94del MANE Select	ENSP00000371532.2:n.1822+93_1822+94del
ENST00000478776.2:n.1360_1361del
ENST00000679488.1:n.405_406del
ENST00000679718.1:n.1058+93_1058+94del
ENST00000679750.1:n.1238+93_1238+94del
ENST00000679780.1:n.76_77del
ENST00000679851.1:n.2099_2100del
ENST00000680021.1:n.2022+93_2022+94del
ENST00000680043.1:c.1374+93_1374+94del
ENST00000680219.1:c.1389+93_1389+94del
ENST00000680243.1:c.*1601+93_*1601+94del	ENSP00000505911.1:n.*1601+93_*1601+94del
ENST00000680296.1:c.1248+93_1248+94del
ENST00000680332.1:n.933_934del
ENST00000680746.1:c.1699+93_1699+94del	ENSP00000505030.1:n.1699+93_1699+94del
ENST00000680751.1:n.1227+93_1227+94del
ENST00000680891.1:c.*1614+93_*1614+94del	ENSP00000505167.1:n.*1614+93_*1614+94del
ENST00000680975.1:n.1207+93_1207+94del
ENST00000681087.1:n.1267+93_1267+94del
ENST00000681306.1:c.1822+93_1822+94del	ENSP00000506072.1:n.1822+93_1822+94del
ENST00000681618.1:c.1699+93_1699+94del	ENSP00000505773.1:n.1699+93_1699+94del
ENST00000681644.1:c.*1494+93_*1494+94del	ENSP00000505180.1:n.*1494+93_*1494+94del
ENST00000681806.1:c.*260+93_*260+94del	ENSP00000505282.1:n.*260+93_*260+94del
ENST00000681942.1:c.1305+93_1305+94del
ENST00000382099.2:c.1822+93_1822+94del	ENSP00000371531.2:n.1822+93_1822+94del
ENST00000382100.7:c.1822+93_1822+94del	ENSP00000371532.2:n.1822+93_1822+94del
ENST00000478776.1:n.427_428del
NM_001018056.1:c.1822+93_1822+94del	NP_001018066.1:n.1822+93_1822+94del
NM_003383.3:c.1822+93_1822+94del	NP_003374.3:n.1822+93_1822+94del
XM_011518029.1:c.1699+93_1699+94del	XP_011516331.1:n.1699+93_1699+94del
NM_001018056.2:c.1822+93_1822+94del	NP_001018066.1:n.1822+93_1822+94del
NM_001322225.1:c.1699+93_1699+94del	NP_001309154.1:n.1699+93_1699+94del
NM_001322226.1:c.1699+93_1699+94del	NP_001309155.1:n.1699+93_1699+94del
NM_003383.4:c.1822+93_1822+94del	NP_003374.3:n.1822+93_1822+94del
XR_001746373.2:n.2161+93_2161+94del
XR_002956805.1:n.2161+93_2161+94del
NM_003383.5:c.1822+93_1822+94del MANE Select	NP_003374.3:n.1822+93_1822+94del
NM_001018056.3:c.1822+93_1822+94del	NP_001018066.1:n.1822+93_1822+94del
NM_001322225.2:c.1699+93_1699+94del	NP_001309154.1:n.1699+93_1699+94del
NM_001322226.2:c.1699+93_1699+94del	NP_001309155.1:n.1699+93_1699+94del