Canonical Allele Identifier: CA463852802

Gene: VLDLR

Linked Data

• ClinVar Variation Id: 2861625
• ClinVar RCV Id: RCV003704435
• MyVariant Identifiers: chr9:g.2643179C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643179C>G , CM000671.2:g.2643179C>G	GRCh38
NC_000009.11:g.2643179C>G , CM000671.1:g.2643179C>G	GRCh37
NC_000009.10:g.2633179C>G	NCBI36
NG_012741.1:g.26387C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382099.3:c.20C>G
ENST00000382100.8:c.468C>G MANE Select	ENSP00000371532.2:p.Pro156=
ENST00000679851.1:n.453C>G
ENST00000680021.1:n.668C>G
ENST00000680043.1:c.20C>G
ENST00000680219.1:c.20C>G
ENST00000680243.1:c.*247C>G	ENSP00000505911.1:n.*247C>G
ENST00000680296.1:c.20C>G
ENST00000680746.1:c.345C>G	ENSP00000505030.1:p.Pro115=
ENST00000680891.1:c.*260C>G	ENSP00000505167.1:n.*260C>G
ENST00000681306.1:c.468C>G	ENSP00000506072.1:p.Pro156=
ENST00000681618.1:c.345C>G	ENSP00000505773.1:p.Pro115=
ENST00000681644.1:c.*140C>G	ENSP00000505180.1:n.*140C>G
ENST00000681806.1:c.468C>G	ENSP00000505282.1:p.Pro156=
ENST00000681942.1:c.20C>G
ENST00000382096.5:c.345C>G	ENSP00000371528.1:p.Pro115=
ENST00000382099.2:c.468C>G	ENSP00000371531.2:p.Pro156=
ENST00000382100.7:c.468C>G	ENSP00000371532.2:p.Pro156=
NM_001018056.1:c.468C>G	NP_001018066.1:p.Pro156=
NM_003383.3:c.468C>G	NP_003374.3:p.Pro156=
XM_011518029.1:c.345C>G	XP_011516331.1:p.Pro115=
NM_001018056.2:c.468C>G	NP_001018066.1:p.Pro156=
NM_001322225.1:c.345C>G	NP_001309154.1:p.Pro115=
NM_001322226.1:c.345C>G	NP_001309155.1:p.Pro115=
NM_003383.4:c.468C>G	NP_003374.3:p.Pro156=
XR_001746373.2:n.872C>G
XR_002956805.1:n.872C>G
NM_003383.5:c.468C>G MANE Select	NP_003374.3:p.Pro156=
NM_001018056.3:c.468C>G	NP_001018066.1:p.Pro156=
NM_001322225.2:c.345C>G	NP_001309154.1:p.Pro115=
NM_001322226.2:c.345C>G	NP_001309155.1:p.Pro115=