Canonical Allele Identifier: CA4964957

Gene: VLDLR

Linked Data

• dbSNP Id: rs772644620
• ExAC: 9:2647635 CATA / C
• gnomAD v2: 9-2647635-CATA-C
• gnomAD v3: 9-2647635-CATA-C
• gnomAD v4: 9-2647635-CATA-C
• MyVariant Identifiers: chr9:g.2647636_2647638del (hg19) ; chr9:g.2647636_2647638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647636_2647638del , CM000671.2:g.2647636_2647638del	GRCh38
NC_000009.11:g.2647636_2647638del , CM000671.1:g.2647636_2647638del	GRCh37
NC_000009.10:g.2637636_2637638del	NCBI36
NG_012741.1:g.30844_30846del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1380+44_1380+46del
ENST00000382100.8:c.1822+44_1822+46del MANE Select	ENSP00000371532.2:n.1822+44_1822+46del
ENST00000478776.2:n.1311_1313del
ENST00000679488.1:n.356_358del
ENST00000679718.1:n.1058+44_1058+46del
ENST00000679750.1:n.1238+44_1238+46del
ENST00000679780.1:n.27_29del
ENST00000679851.1:n.2050_2052del
ENST00000680021.1:n.2022+44_2022+46del
ENST00000680043.1:c.1374+44_1374+46del
ENST00000680219.1:c.1389+44_1389+46del
ENST00000680243.1:c.*1601+44_*1601+46del	ENSP00000505911.1:n.*1601+44_*1601+46del
ENST00000680296.1:c.1248+44_1248+46del
ENST00000680332.1:n.884_886del
ENST00000680746.1:c.1699+44_1699+46del	ENSP00000505030.1:n.1699+44_1699+46del
ENST00000680751.1:n.1227+44_1227+46del
ENST00000680891.1:c.*1614+44_*1614+46del	ENSP00000505167.1:n.*1614+44_*1614+46del
ENST00000680975.1:n.1207+44_1207+46del
ENST00000681087.1:n.1267+44_1267+46del
ENST00000681306.1:c.1822+44_1822+46del	ENSP00000506072.1:n.1822+44_1822+46del
ENST00000681618.1:c.1699+44_1699+46del	ENSP00000505773.1:n.1699+44_1699+46del
ENST00000681644.1:c.*1494+44_*1494+46del	ENSP00000505180.1:n.*1494+44_*1494+46del
ENST00000681806.1:c.*260+44_*260+46del	ENSP00000505282.1:n.*260+44_*260+46del
ENST00000681942.1:c.1305+44_1305+46del
ENST00000382099.2:c.1822+44_1822+46del	ENSP00000371531.2:n.1822+44_1822+46del
ENST00000382100.7:c.1822+44_1822+46del	ENSP00000371532.2:n.1822+44_1822+46del
ENST00000478776.1:n.378_380del
NM_001018056.1:c.1822+44_1822+46del	NP_001018066.1:n.1822+44_1822+46del
NM_003383.3:c.1822+44_1822+46del	NP_003374.3:n.1822+44_1822+46del
XM_011518029.1:c.1699+44_1699+46del	XP_011516331.1:n.1699+44_1699+46del
NM_001018056.2:c.1822+44_1822+46del	NP_001018066.1:n.1822+44_1822+46del
NM_001322225.1:c.1699+44_1699+46del	NP_001309154.1:n.1699+44_1699+46del
NM_001322226.1:c.1699+44_1699+46del	NP_001309155.1:n.1699+44_1699+46del
NM_003383.4:c.1822+44_1822+46del	NP_003374.3:n.1822+44_1822+46del
XR_001746373.2:n.2161+44_2161+46del
XR_002956805.1:n.2161+44_2161+46del
NM_003383.5:c.1822+44_1822+46del MANE Select	NP_003374.3:n.1822+44_1822+46del
NM_001018056.3:c.1822+44_1822+46del	NP_001018066.1:n.1822+44_1822+46del
NM_001322225.2:c.1699+44_1699+46del	NP_001309154.1:n.1699+44_1699+46del
NM_001322226.2:c.1699+44_1699+46del	NP_001309155.1:n.1699+44_1699+46del