Canonical Allele Identifier: CA1828246463
Gene: VLDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2647580G= , CM000671.2:g.2647580G= GRCh38
NC_000009.11:g.2647580G= , CM000671.1:g.2647580G= GRCh37
NC_000009.10:g.2637580G= NCBI36
NG_012741.1:g.30788G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382099.3:c.1368G=
ENST00000382100.8:c.1810G= MANE Select ENSP00000371532.2:p.Gly604=
ENST00000478776.2:n.1255G=
ENST00000679488.1:n.300G=
ENST00000679718.1:n.1046G=
ENST00000679750.1:n.1226G=
ENST00000679851.1:n.1994G=
ENST00000680021.1:n.2010G=
ENST00000680043.1:c.1362G=
ENST00000680219.1:c.1377G=
ENST00000680243.1:c.*1589G= ENSP00000505911.1:n.*1589G=
ENST00000680296.1:c.1236G=
ENST00000680332.1:n.828G=
ENST00000680746.1:c.1687G= ENSP00000505030.1:p.Gly563=
ENST00000680751.1:n.1215G=
ENST00000680891.1:c.*1602G= ENSP00000505167.1:n.*1602G=
ENST00000680975.1:n.1195G=
ENST00000681087.1:n.1255G=
ENST00000681306.1:c.1810G= ENSP00000506072.1:p.Gly604=
ENST00000681618.1:c.1687G= ENSP00000505773.1:p.Gly563=
ENST00000681644.1:c.*1482G= ENSP00000505180.1:n.*1482G=
ENST00000681806.1:c.*248G= ENSP00000505282.1:n.*248G=
ENST00000681942.1:c.1293G=
ENST00000382099.2:c.1810G= ENSP00000371531.2:p.Gly604=
ENST00000382100.7:c.1810G= ENSP00000371532.2:p.Gly604=
ENST00000478776.1:n.322G=
NM_001018056.1:c.1810G= NP_001018066.1:p.Gly604=
NM_003383.3:c.1810G= NP_003374.3:p.Gly604=
XM_011518029.1:c.1687G= XP_011516331.1:p.Gly563=
NM_001018056.2:c.1810G= NP_001018066.1:p.Gly604=
NM_001322225.1:c.1687G= NP_001309154.1:p.Gly563=
NM_001322226.1:c.1687G= NP_001309155.1:p.Gly563=
NM_003383.4:c.1810G= NP_003374.3:p.Gly604=
XR_001746373.2:n.2149G=
XR_002956805.1:n.2149G=
NM_003383.5:c.1810G= MANE Select NP_003374.3:p.Gly604=
NM_001018056.3:c.1810G= NP_001018066.1:p.Gly604=
NM_001322225.2:c.1687G= NP_001309154.1:p.Gly563=
NM_001322226.2:c.1687G= NP_001309155.1:p.Gly563=