Canonical Allele Identifier: CA463713358

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2647585T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2647585T>C , CM000671.2:g.2647585T>C	GRCh38
NC_000009.11:g.2647585T>C , CM000671.1:g.2647585T>C	GRCh37
NC_000009.10:g.2637585T>C	NCBI36
NG_012741.1:g.30793T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1373T>C
ENST00000382100.8:c.1815T>C MANE Select	ENSP00000371532.2:p.Ile605=
ENST00000478776.2:n.1260T>C
ENST00000679488.1:n.305T>C
ENST00000679718.1:n.1051T>C
ENST00000679750.1:n.1231T>C
ENST00000679851.1:n.1999T>C
ENST00000680021.1:n.2015T>C
ENST00000680043.1:c.1367T>C
ENST00000680219.1:c.1382T>C
ENST00000680243.1:c.*1594T>C	ENSP00000505911.1:n.*1594T>C
ENST00000680296.1:c.1241T>C
ENST00000680332.1:n.833T>C
ENST00000680746.1:c.1692T>C	ENSP00000505030.1:p.Ile564=
ENST00000680751.1:n.1220T>C
ENST00000680891.1:c.*1607T>C	ENSP00000505167.1:n.*1607T>C
ENST00000680975.1:n.1200T>C
ENST00000681087.1:n.1260T>C
ENST00000681306.1:c.1815T>C	ENSP00000506072.1:p.Ile605=
ENST00000681618.1:c.1692T>C	ENSP00000505773.1:p.Ile564=
ENST00000681644.1:c.*1487T>C	ENSP00000505180.1:n.*1487T>C
ENST00000681806.1:c.*253T>C	ENSP00000505282.1:n.*253T>C
ENST00000681942.1:c.1298T>C
ENST00000382099.2:c.1815T>C	ENSP00000371531.2:p.Ile605=
ENST00000382100.7:c.1815T>C	ENSP00000371532.2:p.Ile605=
ENST00000478776.1:n.327T>C
NM_001018056.1:c.1815T>C	NP_001018066.1:p.Ile605=
NM_003383.3:c.1815T>C	NP_003374.3:p.Ile605=
XM_011518029.1:c.1692T>C	XP_011516331.1:p.Ile564=
NM_001018056.2:c.1815T>C	NP_001018066.1:p.Ile605=
NM_001322225.1:c.1692T>C	NP_001309154.1:p.Ile564=
NM_001322226.1:c.1692T>C	NP_001309155.1:p.Ile564=
NM_003383.4:c.1815T>C	NP_003374.3:p.Ile605=
XR_001746373.2:n.2154T>C
XR_002956805.1:n.2154T>C
NM_003383.5:c.1815T>C MANE Select	NP_003374.3:p.Ile605=
NM_001018056.3:c.1815T>C	NP_001018066.1:p.Ile605=
NM_001322225.2:c.1692T>C	NP_001309154.1:p.Ile564=
NM_001322226.2:c.1692T>C	NP_001309155.1:p.Ile564=