Canonical Allele Identifier: CA1828222395
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2640730_2640734delinsTAGAA , CM000671.2:g.2640730_2640734delinsTAGAA GRCh38
NC_000009.11:g.2640730_2640734delinsTAGAA , CM000671.1:g.2640730_2640734delinsTAGAA GRCh37
NC_000009.10:g.2630730_2630734delinsTAGAA NCBI36
NG_012741.1:g.23938_23942delinsTAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382100.8:c.326-647_326-643delinsTAGAA MANE Select ENSP00000371532.2:n.326-647_326-643delinsTAGAA
ENST00000679851.1:n.311-647_311-643delinsTAGAA
ENST00000680021.1:n.526-647_526-643delinsTAGAA
ENST00000680243.1:c.*105-647_*105-643delinsTAGAA ENSP00000505911.1:n.*105-647_*105-643delinsTAGAA
ENST00000680746.1:c.325+749_325+753delinsTAGAA ENSP00000505030.1:n.325+749_325+753delinsTAGAA
ENST00000680891.1:c.*121-647_*121-643delinsTAGAA ENSP00000505167.1:n.*121-647_*121-643delinsTAGAA
ENST00000681306.1:c.326-647_326-643delinsTAGAA ENSP00000506072.1:n.326-647_326-643delinsTAGAA
ENST00000681618.1:c.325+749_325+753delinsTAGAA ENSP00000505773.1:n.325+749_325+753delinsTAGAA
ENST00000681644.1:c.*120+749_*120+753delinsTAGAA ENSP00000505180.1:n.*120+749_*120+753delinsTAGAA
ENST00000681770.1:n.1062_1066delinsTAGAA
ENST00000681806.1:c.326-647_326-643delinsTAGAA ENSP00000505282.1:n.326-647_326-643delinsTAGAA
ENST00000382096.5:c.325+749_325+753delinsTAGAA ENSP00000371528.1:n.325+749_325+753delinsTAGAA
ENST00000382099.2:c.326-647_326-643delinsTAGAA ENSP00000371531.2:n.326-647_326-643delinsTAGAA
ENST00000382100.7:c.326-647_326-643delinsTAGAA ENSP00000371532.2:n.326-647_326-643delinsTAGAA
NM_001018056.1:c.326-647_326-643delinsTAGAA NP_001018066.1:n.326-647_326-643delinsTAGAA
NM_003383.3:c.326-647_326-643delinsTAGAA NP_003374.3:n.326-647_326-643delinsTAGAA
XM_011518029.1:c.325+749_325+753delinsTAGAA XP_011516331.1:n.325+749_325+753delinsTAGAA
NM_001018056.2:c.326-647_326-643delinsTAGAA NP_001018066.1:n.326-647_326-643delinsTAGAA
NM_001322225.1:c.325+749_325+753delinsTAGAA NP_001309154.1:n.325+749_325+753delinsTAGAA
NM_001322226.1:c.325+749_325+753delinsTAGAA NP_001309155.1:n.325+749_325+753delinsTAGAA
NM_003383.4:c.326-647_326-643delinsTAGAA NP_003374.3:n.326-647_326-643delinsTAGAA
XR_001746373.2:n.730-647_730-643delinsTAGAA
XR_002956805.1:n.730-647_730-643delinsTAGAA
NM_003383.5:c.326-647_326-643delinsTAGAA MANE Select NP_003374.3:n.326-647_326-643delinsTAGAA
NM_001018056.3:c.326-647_326-643delinsTAGAA NP_001018066.1:n.326-647_326-643delinsTAGAA
NM_001322225.2:c.325+749_325+753delinsTAGAA NP_001309154.1:n.325+749_325+753delinsTAGAA
NM_001322226.2:c.325+749_325+753delinsTAGAA NP_001309155.1:n.325+749_325+753delinsTAGAA