Canonical Allele Identifier: CA372794364

Gene: VLDLR

Linked Data

• MyVariant Identifiers: chr9:g.2645600A>T (hg19) ; chr9:g.2645600A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645600A>T , CM000671.2:g.2645600A>T	GRCh38
NC_000009.11:g.2645600A>T , CM000671.1:g.2645600A>T	GRCh37
NC_000009.10:g.2635600A>T	NCBI36
NG_012741.1:g.28808A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.897A>T
ENST00000382100.8:c.1339A>T MANE Select	ENSP00000371532.2:p.Asn447Tyr
ENST00000478776.2:n.784A>T
ENST00000679718.1:n.575A>T
ENST00000679750.1:n.755A>T
ENST00000679851.1:n.1523A>T
ENST00000680021.1:n.1539A>T
ENST00000680043.1:c.891A>T
ENST00000680219.1:c.906A>T
ENST00000680243.1:c.*1118A>T	ENSP00000505911.1:n.*1118A>T
ENST00000680296.1:c.765A>T
ENST00000680332.1:n.422A>T
ENST00000680746.1:c.1216A>T	ENSP00000505030.1:p.Asn406Tyr
ENST00000680751.1:n.744A>T
ENST00000680891.1:c.*1131A>T	ENSP00000505167.1:n.*1131A>T
ENST00000680975.1:n.724A>T
ENST00000681087.1:n.784A>T
ENST00000681306.1:c.1339A>T	ENSP00000506072.1:p.Asn447Tyr
ENST00000681618.1:c.1216A>T	ENSP00000505773.1:p.Asn406Tyr
ENST00000681644.1:c.*1011A>T	ENSP00000505180.1:n.*1011A>T
ENST00000681806.1:c.1339A>T	ENSP00000505282.1:p.Asn447Tyr
ENST00000681942.1:c.887A>T
ENST00000382099.2:c.1339A>T	ENSP00000371531.2:p.Asn447Tyr
ENST00000382100.7:c.1339A>T	ENSP00000371532.2:p.Asn447Tyr
NM_001018056.1:c.1339A>T	NP_001018066.1:p.Asn447Tyr
NM_003383.3:c.1339A>T	NP_003374.3:p.Asn447Tyr
XM_011518029.1:c.1216A>T	XP_011516331.1:p.Asn406Tyr
NM_001018056.2:c.1339A>T	NP_001018066.1:p.Asn447Tyr
NM_001322225.1:c.1216A>T	NP_001309154.1:p.Asn406Tyr
NM_001322226.1:c.1216A>T	NP_001309155.1:p.Asn406Tyr
NM_003383.4:c.1339A>T	NP_003374.3:p.Asn447Tyr
XR_001746373.2:n.1743A>T
XR_002956805.1:n.1743A>T
NM_003383.5:c.1339A>T MANE Select	NP_003374.3:p.Asn447Tyr
NM_001018056.3:c.1339A>T	NP_001018066.1:p.Asn447Tyr
NM_001322225.2:c.1216A>T	NP_001309154.1:p.Asn406Tyr
NM_001322226.2:c.1216A>T	NP_001309155.1:p.Asn406Tyr