Canonical Allele Identifier: CA372787586

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2635474C>A (hg19) ; chr9:g.2635474C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2635474C>A , CM000671.2:g.2635474C>A	GRCh38
NC_000009.11:g.2635474C>A , CM000671.1:g.2635474C>A	GRCh37
NC_000009.10:g.2625474C>A	NCBI36
NG_012741.1:g.18682C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382096.6:c.104C>A	ENSP00000371528.2:p.Pro35His
ENST00000382100.8:c.104C>A MANE Select	ENSP00000371532.2:p.Pro35His
ENST00000679851.1:n.89C>A
ENST00000680021.1:n.304C>A
ENST00000680243.1:c.104C>A	ENSP00000505911.1:p.Pro35His
ENST00000680746.1:c.104C>A	ENSP00000505030.1:p.Pro35His
ENST00000680891.1:c.202C>A	ENSP00000505167.1:p.Pro68Thr
ENST00000681306.1:c.104C>A	ENSP00000506072.1:p.Pro35His
ENST00000681618.1:c.104C>A	ENSP00000505773.1:p.Pro35His
ENST00000681644.1:c.202C>A	ENSP00000505180.1:p.Pro68Thr
ENST00000681770.1:n.92C>A
ENST00000681806.1:c.104C>A	ENSP00000505282.1:p.Pro35His
ENST00000382096.5:c.104C>A	ENSP00000371528.1:p.Pro35His
ENST00000382099.2:c.104C>A	ENSP00000371531.2:p.Pro35His
ENST00000382100.7:c.104C>A	ENSP00000371532.2:p.Pro35His
NM_001018056.1:c.104C>A	NP_001018066.1:p.Pro35His
NM_003383.3:c.104C>A	NP_003374.3:p.Pro35His
XM_011518029.1:c.104C>A	XP_011516331.1:p.Pro35His
NM_001018056.2:c.104C>A	NP_001018066.1:p.Pro35His
NM_001322225.1:c.104C>A	NP_001309154.1:p.Pro35His
NM_001322226.1:c.104C>A	NP_001309155.1:p.Pro35His
NM_003383.4:c.104C>A	NP_003374.3:p.Pro35His
XR_001746373.2:n.508C>A
XR_002956805.1:n.508C>A
NM_003383.5:c.104C>A MANE Select	NP_003374.3:p.Pro35His
NM_001018056.3:c.104C>A	NP_001018066.1:p.Pro35His
NM_001322225.2:c.104C>A	NP_001309154.1:p.Pro35His
NM_001322226.2:c.104C>A	NP_001309155.1:p.Pro35His