Canonical Allele Identifier: CA463712671

Gene: VLDLR

Linked Data

• gnomAD v4: 9-2635463-C-T
• MyVariant Identifiers: chr9:g.2635463C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2635463C>T , CM000671.2:g.2635463C>T	GRCh38
NC_000009.11:g.2635463C>T , CM000671.1:g.2635463C>T	GRCh37
NC_000009.10:g.2625463C>T	NCBI36
NG_012741.1:g.18671C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382096.6:c.93C>T	ENSP00000371528.2:p.Ala31=
ENST00000382100.8:c.93C>T MANE Select	ENSP00000371532.2:p.Ala31=
ENST00000679851.1:n.78C>T
ENST00000680021.1:n.293C>T
ENST00000680243.1:c.93C>T	ENSP00000505911.1:p.Ala31=
ENST00000680746.1:c.93C>T	ENSP00000505030.1:p.Ala31=
ENST00000680891.1:c.191C>T	ENSP00000505167.1:p.Pro64Leu
ENST00000681306.1:c.93C>T	ENSP00000506072.1:p.Ala31=
ENST00000681618.1:c.93C>T	ENSP00000505773.1:p.Ala31=
ENST00000681644.1:c.191C>T	ENSP00000505180.1:p.Pro64Leu
ENST00000681770.1:n.81C>T
ENST00000681806.1:c.93C>T	ENSP00000505282.1:p.Ala31=
ENST00000382096.5:c.93C>T	ENSP00000371528.1:p.Ala31=
ENST00000382099.2:c.93C>T	ENSP00000371531.2:p.Ala31=
ENST00000382100.7:c.93C>T	ENSP00000371532.2:p.Ala31=
NM_001018056.1:c.93C>T	NP_001018066.1:p.Ala31=
NM_003383.3:c.93C>T	NP_003374.3:p.Ala31=
XM_011518029.1:c.93C>T	XP_011516331.1:p.Ala31=
NM_001018056.2:c.93C>T	NP_001018066.1:p.Ala31=
NM_001322225.1:c.93C>T	NP_001309154.1:p.Ala31=
NM_001322226.1:c.93C>T	NP_001309155.1:p.Ala31=
NM_003383.4:c.93C>T	NP_003374.3:p.Ala31=
XR_001746373.2:n.497C>T
XR_002956805.1:n.497C>T
NM_003383.5:c.93C>T MANE Select	NP_003374.3:p.Ala31=
NM_001018056.3:c.93C>T	NP_001018066.1:p.Ala31=
NM_001322225.2:c.93C>T	NP_001309154.1:p.Ala31=
NM_001322226.2:c.93C>T	NP_001309155.1:p.Ala31=