Canonical Allele Identifier: CA1120577319

Gene: VLDLR

Linked Data

• dbSNP Id: rs1818052260
• gnomAD v3: 9-2645995-T-TAAA
• gnomAD v4: 9-2645995-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645997_2645998insAAA , CM000671.2:g.2645997_2645998insAAA	GRCh38
NC_000009.11:g.2645997_2645998insAAA , CM000671.1:g.2645997_2645998insAAA	GRCh37
NC_000009.10:g.2635997_2635998insAAA	NCBI36
NG_012741.1:g.29205_29206insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1042+252_1042+253insAAA
ENST00000382100.8:c.1484+252_1484+253insAAA MANE Select	ENSP00000371532.2:n.1484+252_1484+253insAAA
ENST00000478776.2:n.929+252_929+253insAAA
ENST00000679718.1:n.720+252_720+253insAAA
ENST00000679750.1:n.900+252_900+253insAAA
ENST00000679851.1:n.1668+252_1668+253insAAA
ENST00000680021.1:n.1684+252_1684+253insAAA
ENST00000680043.1:c.1036+252_1036+253insAAA
ENST00000680219.1:c.1051+252_1051+253insAAA
ENST00000680243.1:c.*1263+252_*1263+253insAAA	ENSP00000505911.1:n.*1263+252_*1263+253insAAA
ENST00000680296.1:c.910+252_910+253insAAA
ENST00000680332.1:n.567+252_567+253insAAA
ENST00000680746.1:c.1361+252_1361+253insAAA	ENSP00000505030.1:n.1361+252_1361+253insAAA
ENST00000680751.1:n.889+252_889+253insAAA
ENST00000680891.1:c.*1276+252_*1276+253insAAA	ENSP00000505167.1:n.*1276+252_*1276+253insAAA
ENST00000680975.1:n.869+252_869+253insAAA
ENST00000681087.1:n.929+252_929+253insAAA
ENST00000681306.1:c.1484+252_1484+253insAAA	ENSP00000506072.1:n.1484+252_1484+253insAAA
ENST00000681618.1:c.1361+252_1361+253insAAA	ENSP00000505773.1:n.1361+252_1361+253insAAA
ENST00000681644.1:c.*1156+252_*1156+253insAAA	ENSP00000505180.1:n.*1156+252_*1156+253insAAA
ENST00000681806.1:c.1484+252_1484+253insAAA	ENSP00000505282.1:n.1484+252_1484+253insAAA
ENST00000681942.1:c.1032+252_1032+253insAAA
ENST00000382099.2:c.1484+252_1484+253insAAA	ENSP00000371531.2:n.1484+252_1484+253insAAA
ENST00000382100.7:c.1484+252_1484+253insAAA	ENSP00000371532.2:n.1484+252_1484+253insAAA
NM_001018056.1:c.1484+252_1484+253insAAA	NP_001018066.1:n.1484+252_1484+253insAAA
NM_003383.3:c.1484+252_1484+253insAAA	NP_003374.3:n.1484+252_1484+253insAAA
XM_011518029.1:c.1361+252_1361+253insAAA	XP_011516331.1:n.1361+252_1361+253insAAA
NM_001018056.2:c.1484+252_1484+253insAAA	NP_001018066.1:n.1484+252_1484+253insAAA
NM_001322225.1:c.1361+252_1361+253insAAA	NP_001309154.1:n.1361+252_1361+253insAAA
NM_001322226.1:c.1361+252_1361+253insAAA	NP_001309155.1:n.1361+252_1361+253insAAA
NM_003383.4:c.1484+252_1484+253insAAA	NP_003374.3:n.1484+252_1484+253insAAA
XR_001746373.2:n.1888+252_1888+253insAAA
XR_002956805.1:n.1888+252_1888+253insAAA
NM_003383.5:c.1484+252_1484+253insAAA MANE Select	NP_003374.3:n.1484+252_1484+253insAAA
NM_001018056.3:c.1484+252_1484+253insAAA	NP_001018066.1:n.1484+252_1484+253insAAA
NM_001322225.2:c.1361+252_1361+253insAAA	NP_001309154.1:n.1361+252_1361+253insAAA
NM_001322226.2:c.1361+252_1361+253insAAA	NP_001309155.1:n.1361+252_1361+253insAAA