Canonical Allele Identifier: CA1828222391

Gene: VLDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2640722_2640726delinsAAATC , CM000671.2:g.2640722_2640726delinsAAATC	GRCh38
NC_000009.11:g.2640722_2640726delinsAAATC , CM000671.1:g.2640722_2640726delinsAAATC	GRCh37
NC_000009.10:g.2630722_2630726delinsAAATC	NCBI36
NG_012741.1:g.23930_23934delinsAAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382100.8:c.326-655_326-651delinsAAATC MANE Select	ENSP00000371532.2:n.326-655_326-651delinsAAATC
ENST00000679851.1:n.311-655_311-651delinsAAATC
ENST00000680021.1:n.526-655_526-651delinsAAATC
ENST00000680243.1:c.*105-655_*105-651delinsAAATC	ENSP00000505911.1:n.*105-655_*105-651delinsAAATC
ENST00000680746.1:c.325+741_325+745delinsAAATC	ENSP00000505030.1:n.325+741_325+745delinsAAATC
ENST00000680891.1:c.*121-655_*121-651delinsAAATC	ENSP00000505167.1:n.*121-655_*121-651delinsAAATC
ENST00000681306.1:c.326-655_326-651delinsAAATC	ENSP00000506072.1:n.326-655_326-651delinsAAATC
ENST00000681618.1:c.325+741_325+745delinsAAATC	ENSP00000505773.1:n.325+741_325+745delinsAAATC
ENST00000681644.1:c.*120+741_*120+745delinsAAATC	ENSP00000505180.1:n.*120+741_*120+745delinsAAATC
ENST00000681770.1:n.1054_1058delinsAAATC
ENST00000681806.1:c.326-655_326-651delinsAAATC	ENSP00000505282.1:n.326-655_326-651delinsAAATC
ENST00000382096.5:c.325+741_325+745delinsAAATC	ENSP00000371528.1:n.325+741_325+745delinsAAATC
ENST00000382099.2:c.326-655_326-651delinsAAATC	ENSP00000371531.2:n.326-655_326-651delinsAAATC
ENST00000382100.7:c.326-655_326-651delinsAAATC	ENSP00000371532.2:n.326-655_326-651delinsAAATC
NM_001018056.1:c.326-655_326-651delinsAAATC	NP_001018066.1:n.326-655_326-651delinsAAATC
NM_003383.3:c.326-655_326-651delinsAAATC	NP_003374.3:n.326-655_326-651delinsAAATC
XM_011518029.1:c.325+741_325+745delinsAAATC	XP_011516331.1:n.325+741_325+745delinsAAATC
NM_001018056.2:c.326-655_326-651delinsAAATC	NP_001018066.1:n.326-655_326-651delinsAAATC
NM_001322225.1:c.325+741_325+745delinsAAATC	NP_001309154.1:n.325+741_325+745delinsAAATC
NM_001322226.1:c.325+741_325+745delinsAAATC	NP_001309155.1:n.325+741_325+745delinsAAATC
NM_003383.4:c.326-655_326-651delinsAAATC	NP_003374.3:n.326-655_326-651delinsAAATC
XR_001746373.2:n.730-655_730-651delinsAAATC
XR_002956805.1:n.730-655_730-651delinsAAATC
NM_003383.5:c.326-655_326-651delinsAAATC MANE Select	NP_003374.3:n.326-655_326-651delinsAAATC
NM_001018056.3:c.326-655_326-651delinsAAATC	NP_001018066.1:n.326-655_326-651delinsAAATC
NM_001322225.2:c.325+741_325+745delinsAAATC	NP_001309154.1:n.325+741_325+745delinsAAATC
NM_001322226.2:c.325+741_325+745delinsAAATC	NP_001309155.1:n.325+741_325+745delinsAAATC