Canonical Allele Identifier: CA372797123
Gene: VLDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2647586A>G , CM000671.2:g.2647586A>G GRCh38
NC_000009.11:g.2647586A>G , CM000671.1:g.2647586A>G GRCh37
NC_000009.10:g.2637586A>G NCBI36
NG_012741.1:g.30794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382099.3:c.1374A>G
ENST00000382100.8:c.1816A>G MANE Select ENSP00000371532.2:p.Thr606Ala
ENST00000478776.2:n.1261A>G
ENST00000679488.1:n.306A>G
ENST00000679718.1:n.1052A>G
ENST00000679750.1:n.1232A>G
ENST00000679851.1:n.2000A>G
ENST00000680021.1:n.2016A>G
ENST00000680043.1:c.1368A>G
ENST00000680219.1:c.1383A>G
ENST00000680243.1:c.*1595A>G ENSP00000505911.1:n.*1595A>G
ENST00000680296.1:c.1242A>G
ENST00000680332.1:n.834A>G
ENST00000680746.1:c.1693A>G ENSP00000505030.1:p.Thr565Ala
ENST00000680751.1:n.1221A>G
ENST00000680891.1:c.*1608A>G ENSP00000505167.1:n.*1608A>G
ENST00000680975.1:n.1201A>G
ENST00000681087.1:n.1261A>G
ENST00000681306.1:c.1816A>G ENSP00000506072.1:p.Thr606Ala
ENST00000681618.1:c.1693A>G ENSP00000505773.1:p.Thr565Ala
ENST00000681644.1:c.*1488A>G ENSP00000505180.1:n.*1488A>G
ENST00000681806.1:c.*254A>G ENSP00000505282.1:n.*254A>G
ENST00000681942.1:c.1299A>G
ENST00000382099.2:c.1816A>G ENSP00000371531.2:p.Thr606Ala
ENST00000382100.7:c.1816A>G ENSP00000371532.2:p.Thr606Ala
ENST00000478776.1:n.328A>G
NM_001018056.1:c.1816A>G NP_001018066.1:p.Thr606Ala
NM_003383.3:c.1816A>G NP_003374.3:p.Thr606Ala
XM_011518029.1:c.1693A>G XP_011516331.1:p.Thr565Ala
NM_001018056.2:c.1816A>G NP_001018066.1:p.Thr606Ala
NM_001322225.1:c.1693A>G NP_001309154.1:p.Thr565Ala
NM_001322226.1:c.1693A>G NP_001309155.1:p.Thr565Ala
NM_003383.4:c.1816A>G NP_003374.3:p.Thr606Ala
XR_001746373.2:n.2155A>G
XR_002956805.1:n.2155A>G
NM_003383.5:c.1816A>G MANE Select NP_003374.3:p.Thr606Ala
NM_001018056.3:c.1816A>G NP_001018066.1:p.Thr606Ala
NM_001322225.2:c.1693A>G NP_001309154.1:p.Thr565Ala
NM_001322226.2:c.1693A>G NP_001309155.1:p.Thr565Ala