Canonical Allele Identifier: CA1828245607

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2645872_2645878delinsTTAAATC , CM000671.2:g.2645872_2645878delinsTTAAATC	GRCh38
NC_000009.11:g.2645872_2645878delinsTTAAATC , CM000671.1:g.2645872_2645878delinsTTAAATC	GRCh37
NC_000009.10:g.2635872_2635878delinsTTAAATC	NCBI36
NG_012741.1:g.29080_29086delinsTTAAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382099.3:c.1042+127_1042+133delinsTTAAATC
ENST00000382100.8:c.1484+127_1484+133delinsTTAAATC MANE Select	ENSP00000371532.2:n.1484+127_1484+133delinsTTAAATC
ENST00000478776.2:n.929+127_929+133delinsTTAAATC
ENST00000679718.1:n.720+127_720+133delinsTTAAATC
ENST00000679750.1:n.900+127_900+133delinsTTAAATC
ENST00000679851.1:n.1668+127_1668+133delinsTTAAATC
ENST00000680021.1:n.1684+127_1684+133delinsTTAAATC
ENST00000680043.1:c.1036+127_1036+133delinsTTAAATC
ENST00000680219.1:c.1051+127_1051+133delinsTTAAATC
ENST00000680243.1:c.*1263+127_*1263+133delinsTTAAATC	ENSP00000505911.1:n.*1263+127_*1263+133delinsTTAAATC
ENST00000680296.1:c.910+127_910+133delinsTTAAATC
ENST00000680332.1:n.567+127_567+133delinsTTAAATC
ENST00000680746.1:c.1361+127_1361+133delinsTTAAATC	ENSP00000505030.1:n.1361+127_1361+133delinsTTAAATC
ENST00000680751.1:n.889+127_889+133delinsTTAAATC
ENST00000680891.1:c.*1276+127_*1276+133delinsTTAAATC	ENSP00000505167.1:n.*1276+127_*1276+133delinsTTAAATC
ENST00000680975.1:n.869+127_869+133delinsTTAAATC
ENST00000681087.1:n.929+127_929+133delinsTTAAATC
ENST00000681306.1:c.1484+127_1484+133delinsTTAAATC	ENSP00000506072.1:n.1484+127_1484+133delinsTTAAATC
ENST00000681618.1:c.1361+127_1361+133delinsTTAAATC	ENSP00000505773.1:n.1361+127_1361+133delinsTTAAATC
ENST00000681644.1:c.*1156+127_*1156+133delinsTTAAATC	ENSP00000505180.1:n.*1156+127_*1156+133delinsTTAAATC
ENST00000681806.1:c.1484+127_1484+133delinsTTAAATC	ENSP00000505282.1:n.1484+127_1484+133delinsTTAAATC
ENST00000681942.1:c.1032+127_1032+133delinsTTAAATC
ENST00000382099.2:c.1484+127_1484+133delinsTTAAATC	ENSP00000371531.2:n.1484+127_1484+133delinsTTAAATC
ENST00000382100.7:c.1484+127_1484+133delinsTTAAATC	ENSP00000371532.2:n.1484+127_1484+133delinsTTAAATC
NM_001018056.1:c.1484+127_1484+133delinsTTAAATC	NP_001018066.1:n.1484+127_1484+133delinsTTAAATC
NM_003383.3:c.1484+127_1484+133delinsTTAAATC	NP_003374.3:n.1484+127_1484+133delinsTTAAATC
XM_011518029.1:c.1361+127_1361+133delinsTTAAATC	XP_011516331.1:n.1361+127_1361+133delinsTTAAATC
NM_001018056.2:c.1484+127_1484+133delinsTTAAATC	NP_001018066.1:n.1484+127_1484+133delinsTTAAATC
NM_001322225.1:c.1361+127_1361+133delinsTTAAATC	NP_001309154.1:n.1361+127_1361+133delinsTTAAATC
NM_001322226.1:c.1361+127_1361+133delinsTTAAATC	NP_001309155.1:n.1361+127_1361+133delinsTTAAATC
NM_003383.4:c.1484+127_1484+133delinsTTAAATC	NP_003374.3:n.1484+127_1484+133delinsTTAAATC
XR_001746373.2:n.1888+127_1888+133delinsTTAAATC
XR_002956805.1:n.1888+127_1888+133delinsTTAAATC
NM_003383.5:c.1484+127_1484+133delinsTTAAATC MANE Select	NP_003374.3:n.1484+127_1484+133delinsTTAAATC
NM_001018056.3:c.1484+127_1484+133delinsTTAAATC	NP_001018066.1:n.1484+127_1484+133delinsTTAAATC
NM_001322225.2:c.1361+127_1361+133delinsTTAAATC	NP_001309154.1:n.1361+127_1361+133delinsTTAAATC
NM_001322226.2:c.1361+127_1361+133delinsTTAAATC	NP_001309155.1:n.1361+127_1361+133delinsTTAAATC