Canonical Allele Identifier: CA372794588

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645688C>G (hg19) ; chr9:g.2645688C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645688C>G , CM000671.2:g.2645688C>G	GRCh38
NC_000009.11:g.2645688C>G , CM000671.1:g.2645688C>G	GRCh37
NC_000009.10:g.2635688C>G	NCBI36
NG_012741.1:g.28896C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.985C>G
ENST00000382100.8:c.1427C>G MANE Select	ENSP00000371532.2:p.Ala476Gly
ENST00000478776.2:n.872C>G
ENST00000679718.1:n.663C>G
ENST00000679750.1:n.843C>G
ENST00000679851.1:n.1611C>G
ENST00000680021.1:n.1627C>G
ENST00000680043.1:c.979C>G
ENST00000680219.1:c.994C>G
ENST00000680243.1:c.*1206C>G	ENSP00000505911.1:n.*1206C>G
ENST00000680296.1:c.853C>G
ENST00000680332.1:n.510C>G
ENST00000680746.1:c.1304C>G	ENSP00000505030.1:p.Ala435Gly
ENST00000680751.1:n.832C>G
ENST00000680891.1:c.*1219C>G	ENSP00000505167.1:n.*1219C>G
ENST00000680975.1:n.812C>G
ENST00000681087.1:n.872C>G
ENST00000681306.1:c.1427C>G	ENSP00000506072.1:p.Ala476Gly
ENST00000681618.1:c.1304C>G	ENSP00000505773.1:p.Ala435Gly
ENST00000681644.1:c.*1099C>G	ENSP00000505180.1:n.*1099C>G
ENST00000681806.1:c.1427C>G	ENSP00000505282.1:p.Ala476Gly
ENST00000681942.1:c.975C>G
ENST00000382099.2:c.1427C>G	ENSP00000371531.2:p.Ala476Gly
ENST00000382100.7:c.1427C>G	ENSP00000371532.2:p.Ala476Gly
NM_001018056.1:c.1427C>G	NP_001018066.1:p.Ala476Gly
NM_003383.3:c.1427C>G	NP_003374.3:p.Ala476Gly
XM_011518029.1:c.1304C>G	XP_011516331.1:p.Ala435Gly
NM_001018056.2:c.1427C>G	NP_001018066.1:p.Ala476Gly
NM_001322225.1:c.1304C>G	NP_001309154.1:p.Ala435Gly
NM_001322226.1:c.1304C>G	NP_001309155.1:p.Ala435Gly
NM_003383.4:c.1427C>G	NP_003374.3:p.Ala476Gly
XR_001746373.2:n.1831C>G
XR_002956805.1:n.1831C>G
NM_003383.5:c.1427C>G MANE Select	NP_003374.3:p.Ala476Gly
NM_001018056.3:c.1427C>G	NP_001018066.1:p.Ala476Gly
NM_001322225.2:c.1304C>G	NP_001309154.1:p.Ala435Gly
NM_001322226.2:c.1304C>G	NP_001309155.1:p.Ala435Gly