Canonical Allele Identifier: CA1293259196

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963268_140963270delinsAAC , CM000664.2:g.140963268_140963270delinsAAC	GRCh38
NC_000002.11:g.141720837_141720839delinsAAC , CM000664.1:g.141720837_141720839delinsAAC	GRCh37
NC_000002.10:g.141437307_141437309delinsAAC	NCBI36
NG_051023.1:g.1174194_1174196delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11330_2888-11328delinsGTT MANE Select	ENSP00000374135.3:n.2888-11330_2888-11328delinsGTT
ENST00000389484.7:c.2888-11330_2888-11328delinsGTT	ENSP00000374135.3:n.2888-11330_2888-11328delinsGTT
ENST00000434794.1:c.323-11330_323-11328delinsGTT	ENSP00000413239.1:n.323-11330_323-11328delinsGTT
ENST00000618808.4:c.2546-11330_2546-11328delinsGTT	ENSP00000478868.1:n.2546-11330_2546-11328delinsGTT
NM_018557.2:c.2888-11330_2888-11328delinsGTT	NP_061027.2:n.2888-11330_2888-11328delinsGTT
XM_011511352.1:c.2999-11330_2999-11328delinsGTT	XP_011509654.1:n.2999-11330_2999-11328delinsGTT
XM_017004341.1:c.2498-11330_2498-11328delinsGTT	XP_016859830.1:n.2498-11330_2498-11328delinsGTT
XR_001738778.1:n.4622-11330_4622-11328delinsGTT
NM_018557.3:c.2888-11330_2888-11328delinsGTT MANE Select	NP_061027.2:n.2888-11330_2888-11328delinsGTT