Canonical Allele Identifier: CA463852908

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2643188C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2643188C>T , CM000671.2:g.2643188C>T	GRCh38
NC_000009.11:g.2643188C>T , CM000671.1:g.2643188C>T	GRCh37
NC_000009.10:g.2633188C>T	NCBI36
NG_012741.1:g.26396C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.29C>T
ENST00000382100.8:c.477C>T MANE Select	ENSP00000371532.2:p.Phe159=
ENST00000679851.1:n.462C>T
ENST00000680021.1:n.677C>T
ENST00000680043.1:c.29C>T
ENST00000680219.1:c.29C>T
ENST00000680243.1:c.*256C>T	ENSP00000505911.1:n.*256C>T
ENST00000680296.1:c.29C>T
ENST00000680746.1:c.354C>T	ENSP00000505030.1:p.Phe118=
ENST00000680891.1:c.*269C>T	ENSP00000505167.1:n.*269C>T
ENST00000681306.1:c.477C>T	ENSP00000506072.1:p.Phe159=
ENST00000681618.1:c.354C>T	ENSP00000505773.1:p.Phe118=
ENST00000681644.1:c.*149C>T	ENSP00000505180.1:n.*149C>T
ENST00000681806.1:c.477C>T	ENSP00000505282.1:p.Phe159=
ENST00000681942.1:c.29C>T
ENST00000382096.5:c.354C>T	ENSP00000371528.1:p.Phe118=
ENST00000382099.2:c.477C>T	ENSP00000371531.2:p.Phe159=
ENST00000382100.7:c.477C>T	ENSP00000371532.2:p.Phe159=
NM_001018056.1:c.477C>T	NP_001018066.1:p.Phe159=
NM_003383.3:c.477C>T	NP_003374.3:p.Phe159=
XM_011518029.1:c.354C>T	XP_011516331.1:p.Phe118=
NM_001018056.2:c.477C>T	NP_001018066.1:p.Phe159=
NM_001322225.1:c.354C>T	NP_001309154.1:p.Phe118=
NM_001322226.1:c.354C>T	NP_001309155.1:p.Phe118=
NM_003383.4:c.477C>T	NP_003374.3:p.Phe159=
XR_001746373.2:n.881C>T
XR_002956805.1:n.881C>T
NM_003383.5:c.477C>T MANE Select	NP_003374.3:p.Phe159=
NM_001018056.3:c.477C>T	NP_001018066.1:p.Phe159=
NM_001322225.2:c.354C>T	NP_001309154.1:p.Phe118=
NM_001322226.2:c.354C>T	NP_001309155.1:p.Phe118=