Canonical Allele Identifier: CA372797127
Gene: VLDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2647589C>A , CM000671.2:g.2647589C>A GRCh38
NC_000009.11:g.2647589C>A , CM000671.1:g.2647589C>A GRCh37
NC_000009.10:g.2637589C>A NCBI36
NG_012741.1:g.30797C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382099.3:c.1377C>A
ENST00000382100.8:c.1819C>A MANE Select ENSP00000371532.2:p.Leu607Ile
ENST00000478776.2:n.1264C>A
ENST00000679488.1:n.309C>A
ENST00000679718.1:n.1055C>A
ENST00000679750.1:n.1235C>A
ENST00000679851.1:n.2003C>A
ENST00000680021.1:n.2019C>A
ENST00000680043.1:c.1371C>A
ENST00000680219.1:c.1386C>A
ENST00000680243.1:c.*1598C>A ENSP00000505911.1:n.*1598C>A
ENST00000680296.1:c.1245C>A
ENST00000680332.1:n.837C>A
ENST00000680746.1:c.1696C>A ENSP00000505030.1:p.Leu566Ile
ENST00000680751.1:n.1224C>A
ENST00000680891.1:c.*1611C>A ENSP00000505167.1:n.*1611C>A
ENST00000680975.1:n.1204C>A
ENST00000681087.1:n.1264C>A
ENST00000681306.1:c.1819C>A ENSP00000506072.1:p.Leu607Ile
ENST00000681618.1:c.1696C>A ENSP00000505773.1:p.Leu566Ile
ENST00000681644.1:c.*1491C>A ENSP00000505180.1:n.*1491C>A
ENST00000681806.1:c.*257C>A ENSP00000505282.1:n.*257C>A
ENST00000681942.1:c.1302C>A
ENST00000382099.2:c.1819C>A ENSP00000371531.2:p.Leu607Ile
ENST00000382100.7:c.1819C>A ENSP00000371532.2:p.Leu607Ile
ENST00000478776.1:n.331C>A
NM_001018056.1:c.1819C>A NP_001018066.1:p.Leu607Ile
NM_003383.3:c.1819C>A NP_003374.3:p.Leu607Ile
XM_011518029.1:c.1696C>A XP_011516331.1:p.Leu566Ile
NM_001018056.2:c.1819C>A NP_001018066.1:p.Leu607Ile
NM_001322225.1:c.1696C>A NP_001309154.1:p.Leu566Ile
NM_001322226.1:c.1696C>A NP_001309155.1:p.Leu566Ile
NM_003383.4:c.1819C>A NP_003374.3:p.Leu607Ile
XR_001746373.2:n.2158C>A
XR_002956805.1:n.2158C>A
NM_003383.5:c.1819C>A MANE Select NP_003374.3:p.Leu607Ile
NM_001018056.3:c.1819C>A NP_001018066.1:p.Leu607Ile
NM_001322225.2:c.1696C>A NP_001309154.1:p.Leu566Ile
NM_001322226.2:c.1696C>A NP_001309155.1:p.Leu566Ile