Canonical Allele Identifier: CA372797134
Gene: VLDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2647592G>C , CM000671.2:g.2647592G>C GRCh38
NC_000009.11:g.2647592G>C , CM000671.1:g.2647592G>C GRCh37
NC_000009.10:g.2637592G>C NCBI36
NG_012741.1:g.30800G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382099.3:c.1380G>C
ENST00000382100.8:c.1822G>C MANE Select ENSP00000371532.2:p.Asp608His
ENST00000478776.2:n.1267G>C
ENST00000679488.1:n.312G>C
ENST00000679718.1:n.1058G>C
ENST00000679750.1:n.1238G>C
ENST00000679851.1:n.2006G>C
ENST00000680021.1:n.2022G>C
ENST00000680043.1:c.1374G>C
ENST00000680219.1:c.1389G>C
ENST00000680243.1:c.*1601G>C ENSP00000505911.1:n.*1601G>C
ENST00000680296.1:c.1248G>C
ENST00000680332.1:n.840G>C
ENST00000680746.1:c.1699G>C ENSP00000505030.1:p.Asp567His
ENST00000680751.1:n.1227G>C
ENST00000680891.1:c.*1614G>C ENSP00000505167.1:n.*1614G>C
ENST00000680975.1:n.1207G>C
ENST00000681087.1:n.1267G>C
ENST00000681306.1:c.1822G>C ENSP00000506072.1:p.Asp608His
ENST00000681618.1:c.1699G>C ENSP00000505773.1:p.Asp567His
ENST00000681644.1:c.*1494G>C ENSP00000505180.1:n.*1494G>C
ENST00000681806.1:c.*260G>C ENSP00000505282.1:n.*260G>C
ENST00000681942.1:c.1305G>C
ENST00000382099.2:c.1822G>C ENSP00000371531.2:p.Asp608His
ENST00000382100.7:c.1822G>C ENSP00000371532.2:p.Asp608His
ENST00000478776.1:n.334G>C
NM_001018056.1:c.1822G>C NP_001018066.1:p.Asp608His
NM_003383.3:c.1822G>C NP_003374.3:p.Asp608His
XM_011518029.1:c.1699G>C XP_011516331.1:p.Asp567His
NM_001018056.2:c.1822G>C NP_001018066.1:p.Asp608His
NM_001322225.1:c.1699G>C NP_001309154.1:p.Asp567His
NM_001322226.1:c.1699G>C NP_001309155.1:p.Asp567His
NM_003383.4:c.1822G>C NP_003374.3:p.Asp608His
XR_001746373.2:n.2161G>C
XR_002956805.1:n.2161G>C
NM_003383.5:c.1822G>C MANE Select NP_003374.3:p.Asp608His
NM_001018056.3:c.1822G>C NP_001018066.1:p.Asp608His
NM_001322225.2:c.1699G>C NP_001309154.1:p.Asp567His
NM_001322226.2:c.1699G>C NP_001309155.1:p.Asp567His