Canonical Allele Identifier: CA1828245425

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645492_2645495delinsGCTC , CM000671.2:g.2645492_2645495delinsGCTC	GRCh38
NC_000009.11:g.2645492_2645495delinsGCTC , CM000671.1:g.2645492_2645495delinsGCTC	GRCh37
NC_000009.10:g.2635492_2635495delinsGCTC	NCBI36
NG_012741.1:g.28700_28703delinsGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.871-82_871-79delinsGCTC
ENST00000382100.8:c.1313-82_1313-79delinsGCTC MANE Select	ENSP00000371532.2:n.1313-82_1313-79delinsGCTC
ENST00000478776.2:n.758-82_758-79delinsGCTC
ENST00000679718.1:n.549-82_549-79delinsGCTC
ENST00000679750.1:n.729-82_729-79delinsGCTC
ENST00000679851.1:n.1497-82_1497-79delinsGCTC
ENST00000680021.1:n.1513-82_1513-79delinsGCTC
ENST00000680043.1:c.865-82_865-79delinsGCTC
ENST00000680219.1:c.865-67_865-64delinsGCTC
ENST00000680243.1:c.*1092-82_*1092-79delinsGCTC	ENSP00000505911.1:n.*1092-82_*1092-79delinsGCTC
ENST00000680296.1:c.739-82_739-79delinsGCTC
ENST00000680332.1:n.396-82_396-79delinsGCTC
ENST00000680746.1:c.1190-82_1190-79delinsGCTC	ENSP00000505030.1:n.1190-82_1190-79delinsGCTC
ENST00000680751.1:n.718-82_718-79delinsGCTC
ENST00000680891.1:c.*1105-82_*1105-79delinsGCTC	ENSP00000505167.1:n.*1105-82_*1105-79delinsGCTC
ENST00000680975.1:n.698-82_698-79delinsGCTC
ENST00000681087.1:n.758-82_758-79delinsGCTC
ENST00000681306.1:c.1313-82_1313-79delinsGCTC	ENSP00000506072.1:n.1313-82_1313-79delinsGCTC
ENST00000681618.1:c.1190-82_1190-79delinsGCTC	ENSP00000505773.1:n.1190-82_1190-79delinsGCTC
ENST00000681644.1:c.*985-82_*985-79delinsGCTC	ENSP00000505180.1:n.*985-82_*985-79delinsGCTC
ENST00000681806.1:c.1313-82_1313-79delinsGCTC	ENSP00000505282.1:n.1313-82_1313-79delinsGCTC
ENST00000681942.1:c.861-82_861-79delinsGCTC
ENST00000382099.2:c.1313-82_1313-79delinsGCTC	ENSP00000371531.2:n.1313-82_1313-79delinsGCTC
ENST00000382100.7:c.1313-82_1313-79delinsGCTC	ENSP00000371532.2:n.1313-82_1313-79delinsGCTC
NM_001018056.1:c.1313-82_1313-79delinsGCTC	NP_001018066.1:n.1313-82_1313-79delinsGCTC
NM_003383.3:c.1313-82_1313-79delinsGCTC	NP_003374.3:n.1313-82_1313-79delinsGCTC
XM_011518029.1:c.1190-82_1190-79delinsGCTC	XP_011516331.1:n.1190-82_1190-79delinsGCTC
NM_001018056.2:c.1313-82_1313-79delinsGCTC	NP_001018066.1:n.1313-82_1313-79delinsGCTC
NM_001322225.1:c.1190-82_1190-79delinsGCTC	NP_001309154.1:n.1190-82_1190-79delinsGCTC
NM_001322226.1:c.1190-82_1190-79delinsGCTC	NP_001309155.1:n.1190-82_1190-79delinsGCTC
NM_003383.4:c.1313-82_1313-79delinsGCTC	NP_003374.3:n.1313-82_1313-79delinsGCTC
XR_001746373.2:n.1717-82_1717-79delinsGCTC
XR_002956805.1:n.1717-82_1717-79delinsGCTC
NM_003383.5:c.1313-82_1313-79delinsGCTC MANE Select	NP_003374.3:n.1313-82_1313-79delinsGCTC
NM_001018056.3:c.1313-82_1313-79delinsGCTC	NP_001018066.1:n.1313-82_1313-79delinsGCTC
NM_001322225.2:c.1190-82_1190-79delinsGCTC	NP_001309154.1:n.1190-82_1190-79delinsGCTC
NM_001322226.2:c.1190-82_1190-79delinsGCTC	NP_001309155.1:n.1190-82_1190-79delinsGCTC