Canonical Allele Identifier: CA463712665

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2635454G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2635454G>T , CM000671.2:g.2635454G>T	GRCh38
NC_000009.11:g.2635454G>T , CM000671.1:g.2635454G>T	GRCh37
NC_000009.10:g.2625454G>T	NCBI36
NG_012741.1:g.18662G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382096.6:c.84G>T	ENSP00000371528.2:p.Gly28=
ENST00000382100.8:c.84G>T MANE Select	ENSP00000371532.2:p.Gly28=
ENST00000679851.1:n.69G>T
ENST00000680021.1:n.284G>T
ENST00000680243.1:c.84G>T	ENSP00000505911.1:p.Gly28=
ENST00000680746.1:c.84G>T	ENSP00000505030.1:p.Gly28=
ENST00000680891.1:c.182G>T	ENSP00000505167.1:p.Gly61Val
ENST00000681306.1:c.84G>T	ENSP00000506072.1:p.Gly28=
ENST00000681618.1:c.84G>T	ENSP00000505773.1:p.Gly28=
ENST00000681644.1:c.182G>T	ENSP00000505180.1:p.Gly61Val
ENST00000681770.1:n.72G>T
ENST00000681806.1:c.84G>T	ENSP00000505282.1:p.Gly28=
ENST00000382096.5:c.84G>T	ENSP00000371528.1:p.Gly28=
ENST00000382099.2:c.84G>T	ENSP00000371531.2:p.Gly28=
ENST00000382100.7:c.84G>T	ENSP00000371532.2:p.Gly28=
NM_001018056.1:c.84G>T	NP_001018066.1:p.Gly28=
NM_003383.3:c.84G>T	NP_003374.3:p.Gly28=
XM_011518029.1:c.84G>T	XP_011516331.1:p.Gly28=
NM_001018056.2:c.84G>T	NP_001018066.1:p.Gly28=
NM_001322225.1:c.84G>T	NP_001309154.1:p.Gly28=
NM_001322226.1:c.84G>T	NP_001309155.1:p.Gly28=
NM_003383.4:c.84G>T	NP_003374.3:p.Gly28=
XR_001746373.2:n.488G>T
XR_002956805.1:n.488G>T
NM_003383.5:c.84G>T MANE Select	NP_003374.3:p.Gly28=
NM_001018056.3:c.84G>T	NP_001018066.1:p.Gly28=
NM_001322225.2:c.84G>T	NP_001309154.1:p.Gly28=
NM_001322226.2:c.84G>T	NP_001309155.1:p.Gly28=