Canonical Allele Identifier: CA2782683096
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2645495_2645511del , CM000671.2:g.2645495_2645511del GRCh38
NC_000009.11:g.2645495_2645511del , CM000671.1:g.2645495_2645511del GRCh37
NC_000009.10:g.2635495_2635511del NCBI36
NG_012741.1:g.28703_28719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382099.3:c.871-79_871-63del
ENST00000382100.8:c.1313-79_1313-63del MANE Select ENSP00000371532.2:n.1313-79_1313-63del
ENST00000478776.2:n.758-79_758-63del
ENST00000679718.1:n.549-79_549-63del
ENST00000679750.1:n.729-79_729-63del
ENST00000679851.1:n.1497-79_1497-63del
ENST00000680021.1:n.1513-79_1513-63del
ENST00000680043.1:c.865-79_865-63del
ENST00000680219.1:c.865-64_865-48del
ENST00000680243.1:c.*1092-79_*1092-63del ENSP00000505911.1:n.*1092-79_*1092-63del
ENST00000680296.1:c.739-79_739-63del
ENST00000680332.1:n.396-79_396-63del
ENST00000680746.1:c.1190-79_1190-63del ENSP00000505030.1:n.1190-79_1190-63del
ENST00000680751.1:n.718-79_718-63del
ENST00000680891.1:c.*1105-79_*1105-63del ENSP00000505167.1:n.*1105-79_*1105-63del
ENST00000680975.1:n.698-79_698-63del
ENST00000681087.1:n.758-79_758-63del
ENST00000681306.1:c.1313-79_1313-63del ENSP00000506072.1:n.1313-79_1313-63del
ENST00000681618.1:c.1190-79_1190-63del ENSP00000505773.1:n.1190-79_1190-63del
ENST00000681644.1:c.*985-79_*985-63del ENSP00000505180.1:n.*985-79_*985-63del
ENST00000681806.1:c.1313-79_1313-63del ENSP00000505282.1:n.1313-79_1313-63del
ENST00000681942.1:c.861-79_861-63del
ENST00000382099.2:c.1313-79_1313-63del ENSP00000371531.2:n.1313-79_1313-63del
ENST00000382100.7:c.1313-79_1313-63del ENSP00000371532.2:n.1313-79_1313-63del
NM_001018056.1:c.1313-79_1313-63del NP_001018066.1:n.1313-79_1313-63del
NM_003383.3:c.1313-79_1313-63del NP_003374.3:n.1313-79_1313-63del
XM_011518029.1:c.1190-79_1190-63del XP_011516331.1:n.1190-79_1190-63del
NM_001018056.2:c.1313-79_1313-63del NP_001018066.1:n.1313-79_1313-63del
NM_001322225.1:c.1190-79_1190-63del NP_001309154.1:n.1190-79_1190-63del
NM_001322226.1:c.1190-79_1190-63del NP_001309155.1:n.1190-79_1190-63del
NM_003383.4:c.1313-79_1313-63del NP_003374.3:n.1313-79_1313-63del
XR_001746373.2:n.1717-79_1717-63del
XR_002956805.1:n.1717-79_1717-63del
NM_003383.5:c.1313-79_1313-63del MANE Select NP_003374.3:n.1313-79_1313-63del
NM_001018056.3:c.1313-79_1313-63del NP_001018066.1:n.1313-79_1313-63del
NM_001322225.2:c.1190-79_1190-63del NP_001309154.1:n.1190-79_1190-63del
NM_001322226.2:c.1190-79_1190-63del NP_001309155.1:n.1190-79_1190-63del