Canonical Allele Identifier: CA372793359

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2644735T>G (hg19) ; chr9:g.2644735T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2644735T>G , CM000671.2:g.2644735T>G	GRCh38
NC_000009.11:g.2644735T>G , CM000671.1:g.2644735T>G	GRCh37
NC_000009.10:g.2634735T>G	NCBI36
NG_012741.1:g.27943T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382099.3:c.626T>G
ENST00000382100.8:c.1068T>G MANE Select	ENSP00000371532.2:p.His356Gln
ENST00000478776.2:n.410T>G
ENST00000679718.1:n.201T>G
ENST00000679750.1:n.381T>G
ENST00000679851.1:n.1149T>G
ENST00000680021.1:n.1268T>G
ENST00000680043.1:c.620T>G
ENST00000680150.1:n.248T>G
ENST00000680219.1:c.620T>G
ENST00000680243.1:c.*847T>G	ENSP00000505911.1:n.*847T>G
ENST00000680296.1:c.620T>G
ENST00000680332.1:n.48T>G
ENST00000680746.1:c.945T>G	ENSP00000505030.1:p.His315Gln
ENST00000680751.1:n.370T>G
ENST00000680891.1:c.*860T>G	ENSP00000505167.1:n.*860T>G
ENST00000680975.1:n.350T>G
ENST00000681087.1:n.410T>G
ENST00000681306.1:c.1068T>G	ENSP00000506072.1:p.His356Gln
ENST00000681618.1:c.945T>G	ENSP00000505773.1:p.His315Gln
ENST00000681644.1:c.*740T>G	ENSP00000505180.1:n.*740T>G
ENST00000681806.1:c.1068T>G	ENSP00000505282.1:p.His356Gln
ENST00000681942.1:c.620T>G
ENST00000382099.2:c.1068T>G	ENSP00000371531.2:p.His356Gln
ENST00000382100.7:c.1068T>G	ENSP00000371532.2:p.His356Gln
NM_001018056.1:c.1068T>G	NP_001018066.1:p.His356Gln
NM_003383.3:c.1068T>G	NP_003374.3:p.His356Gln
XM_011518029.1:c.945T>G	XP_011516331.1:p.His315Gln
NM_001018056.2:c.1068T>G	NP_001018066.1:p.His356Gln
NM_001322225.1:c.945T>G	NP_001309154.1:p.His315Gln
NM_001322226.1:c.945T>G	NP_001309155.1:p.His315Gln
NM_003383.4:c.1068T>G	NP_003374.3:p.His356Gln
XR_001746373.2:n.1472T>G
XR_002956805.1:n.1472T>G
NM_003383.5:c.1068T>G MANE Select	NP_003374.3:p.His356Gln
NM_001018056.3:c.1068T>G	NP_001018066.1:p.His356Gln
NM_001322225.2:c.945T>G	NP_001309154.1:p.His315Gln
NM_001322226.2:c.945T>G	NP_001309155.1:p.His315Gln