Canonical Allele Identifier: CA372794517

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645655T>A (hg19) ; chr9:g.2645655T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645655T>A , CM000671.2:g.2645655T>A	GRCh38
NC_000009.11:g.2645655T>A , CM000671.1:g.2645655T>A	GRCh37
NC_000009.10:g.2635655T>A	NCBI36
NG_012741.1:g.28863T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.952T>A
ENST00000382100.8:c.1394T>A MANE Select	ENSP00000371532.2:p.Val465Asp
ENST00000478776.2:n.839T>A
ENST00000679718.1:n.630T>A
ENST00000679750.1:n.810T>A
ENST00000679851.1:n.1578T>A
ENST00000680021.1:n.1594T>A
ENST00000680043.1:c.946T>A
ENST00000680219.1:c.961T>A
ENST00000680243.1:c.*1173T>A	ENSP00000505911.1:n.*1173T>A
ENST00000680296.1:c.820T>A
ENST00000680332.1:n.477T>A
ENST00000680746.1:c.1271T>A	ENSP00000505030.1:p.Val424Asp
ENST00000680751.1:n.799T>A
ENST00000680891.1:c.*1186T>A	ENSP00000505167.1:n.*1186T>A
ENST00000680975.1:n.779T>A
ENST00000681087.1:n.839T>A
ENST00000681306.1:c.1394T>A	ENSP00000506072.1:p.Val465Asp
ENST00000681618.1:c.1271T>A	ENSP00000505773.1:p.Val424Asp
ENST00000681644.1:c.*1066T>A	ENSP00000505180.1:n.*1066T>A
ENST00000681806.1:c.1394T>A	ENSP00000505282.1:p.Val465Asp
ENST00000681942.1:c.942T>A
ENST00000382099.2:c.1394T>A	ENSP00000371531.2:p.Val465Asp
ENST00000382100.7:c.1394T>A	ENSP00000371532.2:p.Val465Asp
NM_001018056.1:c.1394T>A	NP_001018066.1:p.Val465Asp
NM_003383.3:c.1394T>A	NP_003374.3:p.Val465Asp
XM_011518029.1:c.1271T>A	XP_011516331.1:p.Val424Asp
NM_001018056.2:c.1394T>A	NP_001018066.1:p.Val465Asp
NM_001322225.1:c.1271T>A	NP_001309154.1:p.Val424Asp
NM_001322226.1:c.1271T>A	NP_001309155.1:p.Val424Asp
NM_003383.4:c.1394T>A	NP_003374.3:p.Val465Asp
XR_001746373.2:n.1798T>A
XR_002956805.1:n.1798T>A
NM_003383.5:c.1394T>A MANE Select	NP_003374.3:p.Val465Asp
NM_001018056.3:c.1394T>A	NP_001018066.1:p.Val465Asp
NM_001322225.2:c.1271T>A	NP_001309154.1:p.Val424Asp
NM_001322226.2:c.1271T>A	NP_001309155.1:p.Val424Asp