Canonical Allele Identifier: CA372794315

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645589T>G (hg19) ; chr9:g.2645589T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645589T>G , CM000671.2:g.2645589T>G	GRCh38
NC_000009.11:g.2645589T>G , CM000671.1:g.2645589T>G	GRCh37
NC_000009.10:g.2635589T>G	NCBI36
NG_012741.1:g.28797T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.886T>G
ENST00000382100.8:c.1328T>G MANE Select	ENSP00000371532.2:p.Leu443Arg
ENST00000478776.2:n.773T>G
ENST00000679718.1:n.564T>G
ENST00000679750.1:n.744T>G
ENST00000679851.1:n.1512T>G
ENST00000680021.1:n.1528T>G
ENST00000680043.1:c.880T>G
ENST00000680219.1:c.895T>G
ENST00000680243.1:c.*1107T>G	ENSP00000505911.1:n.*1107T>G
ENST00000680296.1:c.754T>G
ENST00000680332.1:n.411T>G
ENST00000680746.1:c.1205T>G	ENSP00000505030.1:p.Leu402Arg
ENST00000680751.1:n.733T>G
ENST00000680891.1:c.*1120T>G	ENSP00000505167.1:n.*1120T>G
ENST00000680975.1:n.713T>G
ENST00000681087.1:n.773T>G
ENST00000681306.1:c.1328T>G	ENSP00000506072.1:p.Leu443Arg
ENST00000681618.1:c.1205T>G	ENSP00000505773.1:p.Leu402Arg
ENST00000681644.1:c.*1000T>G	ENSP00000505180.1:n.*1000T>G
ENST00000681806.1:c.1328T>G	ENSP00000505282.1:p.Leu443Arg
ENST00000681942.1:c.876T>G
ENST00000382099.2:c.1328T>G	ENSP00000371531.2:p.Leu443Arg
ENST00000382100.7:c.1328T>G	ENSP00000371532.2:p.Leu443Arg
NM_001018056.1:c.1328T>G	NP_001018066.1:p.Leu443Arg
NM_003383.3:c.1328T>G	NP_003374.3:p.Leu443Arg
XM_011518029.1:c.1205T>G	XP_011516331.1:p.Leu402Arg
NM_001018056.2:c.1328T>G	NP_001018066.1:p.Leu443Arg
NM_001322225.1:c.1205T>G	NP_001309154.1:p.Leu402Arg
NM_001322226.1:c.1205T>G	NP_001309155.1:p.Leu402Arg
NM_003383.4:c.1328T>G	NP_003374.3:p.Leu443Arg
XR_001746373.2:n.1732T>G
XR_002956805.1:n.1732T>G
NM_003383.5:c.1328T>G MANE Select	NP_003374.3:p.Leu443Arg
NM_001018056.3:c.1328T>G	NP_001018066.1:p.Leu443Arg
NM_001322225.2:c.1205T>G	NP_001309154.1:p.Leu402Arg
NM_001322226.2:c.1205T>G	NP_001309155.1:p.Leu402Arg