Canonical Allele Identifier: CA463712675
Gene: VLDLR HGNC NCBI

Linked Data

dbSNP Id: rs1156783917
gnomAD v2: 9-2635475-C-A
gnomAD v3: 9-2635475-C-A
gnomAD v4: 9-2635475-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2635475C>A , CM000671.2:g.2635475C>A GRCh38
NC_000009.11:g.2635475C>A , CM000671.1:g.2635475C>A GRCh37
NC_000009.10:g.2625475C>A NCBI36
NG_012741.1:g.18683C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382096.6:c.105C>A ENSP00000371528.2:p.Pro35=
ENST00000382100.8:c.105C>A MANE Select ENSP00000371532.2:p.Pro35=
ENST00000679851.1:n.90C>A
ENST00000680021.1:n.305C>A
ENST00000680243.1:c.105C>A ENSP00000505911.1:p.Pro35=
ENST00000680746.1:c.105C>A ENSP00000505030.1:p.Pro35=
ENST00000680891.1:c.203C>A ENSP00000505167.1:p.Pro68His
ENST00000681306.1:c.105C>A ENSP00000506072.1:p.Pro35=
ENST00000681618.1:c.105C>A ENSP00000505773.1:p.Pro35=
ENST00000681644.1:c.203C>A ENSP00000505180.1:p.Pro68His
ENST00000681770.1:n.93C>A
ENST00000681806.1:c.105C>A ENSP00000505282.1:p.Pro35=
ENST00000382096.5:c.105C>A ENSP00000371528.1:p.Pro35=
ENST00000382099.2:c.105C>A ENSP00000371531.2:p.Pro35=
ENST00000382100.7:c.105C>A ENSP00000371532.2:p.Pro35=
NM_001018056.1:c.105C>A NP_001018066.1:p.Pro35=
NM_003383.3:c.105C>A NP_003374.3:p.Pro35=
XM_011518029.1:c.105C>A XP_011516331.1:p.Pro35=
NM_001018056.2:c.105C>A NP_001018066.1:p.Pro35=
NM_001322225.1:c.105C>A NP_001309154.1:p.Pro35=
NM_001322226.1:c.105C>A NP_001309155.1:p.Pro35=
NM_003383.4:c.105C>A NP_003374.3:p.Pro35=
XR_001746373.2:n.509C>A
XR_002956805.1:n.509C>A
NM_003383.5:c.105C>A MANE Select NP_003374.3:p.Pro35=
NM_001018056.3:c.105C>A NP_001018066.1:p.Pro35=
NM_001322225.2:c.105C>A NP_001309154.1:p.Pro35=
NM_001322226.2:c.105C>A NP_001309155.1:p.Pro35=