Canonical Allele Identifier: CA862625334

Gene: VLDLR

Linked Data

• dbSNP Id: rs1225111299
• gnomAD v3: 9-2642973-TTG-T
• gnomAD v4: 9-2642973-TTG-T
• MyVariant Identifiers: chr9:g.2642974_2642975del (hg19) ; chr9:g.2642974_2642975del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2642978_2642979del , CM000671.2:g.2642978_2642979del	GRCh38
NC_000009.11:g.2642978_2642979del , CM000671.1:g.2642978_2642979del	GRCh37
NC_000009.10:g.2632978_2632979del	NCBI36
NG_012741.1:g.26186_26187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382100.8:c.449-182_449-181del MANE Select	ENSP00000371532.2:n.449-182_449-181del
ENST00000679851.1:n.434-182_434-181del
ENST00000680021.1:n.649-182_649-181del
ENST00000680243.1:c.*228-182_*228-181del	ENSP00000505911.1:n.*228-182_*228-181del
ENST00000680746.1:c.326-182_326-181del	ENSP00000505030.1:n.326-182_326-181del
ENST00000680891.1:c.*241-182_*241-181del	ENSP00000505167.1:n.*241-182_*241-181del
ENST00000681306.1:c.449-182_449-181del	ENSP00000506072.1:n.449-182_449-181del
ENST00000681618.1:c.326-182_326-181del	ENSP00000505773.1:n.326-182_326-181del
ENST00000681644.1:c.*121-182_*121-181del	ENSP00000505180.1:n.*121-182_*121-181del
ENST00000681806.1:c.449-182_449-181del	ENSP00000505282.1:n.449-182_449-181del
ENST00000382096.5:c.326-182_326-181del	ENSP00000371528.1:n.326-182_326-181del
ENST00000382099.2:c.449-182_449-181del	ENSP00000371531.2:n.449-182_449-181del
ENST00000382100.7:c.449-182_449-181del	ENSP00000371532.2:n.449-182_449-181del
NM_001018056.1:c.449-182_449-181del	NP_001018066.1:n.449-182_449-181del
NM_003383.3:c.449-182_449-181del	NP_003374.3:n.449-182_449-181del
XM_011518029.1:c.326-182_326-181del	XP_011516331.1:n.326-182_326-181del
NM_001018056.2:c.449-182_449-181del	NP_001018066.1:n.449-182_449-181del
NM_001322225.1:c.326-182_326-181del	NP_001309154.1:n.326-182_326-181del
NM_001322226.1:c.326-182_326-181del	NP_001309155.1:n.326-182_326-181del
NM_003383.4:c.449-182_449-181del	NP_003374.3:n.449-182_449-181del
XR_001746373.2:n.853-182_853-181del
XR_002956805.1:n.853-182_853-181del
NM_003383.5:c.449-182_449-181del MANE Select	NP_003374.3:n.449-182_449-181del
NM_001018056.3:c.449-182_449-181del	NP_001018066.1:n.449-182_449-181del
NM_001322225.2:c.326-182_326-181del	NP_001309154.1:n.326-182_326-181del
NM_001322226.2:c.326-182_326-181del	NP_001309155.1:n.326-182_326-181del