Canonical Allele Identifier: CA1293259478
Gene: LRP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963450_140963451delinsTA , CM000664.2:g.140963450_140963451delinsTA GRCh38
NC_000002.11:g.141721019_141721020delinsTA , CM000664.1:g.141721019_141721020delinsTA GRCh37
NC_000002.10:g.141437489_141437490delinsTA NCBI36
NG_051023.1:g.1174013_1174014delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11511_2888-11510delinsTA MANE Select ENSP00000374135.3:n.2888-11511_2888-11510delinsTA
ENST00000389484.7:c.2888-11511_2888-11510delinsTA ENSP00000374135.3:n.2888-11511_2888-11510delinsTA
ENST00000434794.1:c.323-11511_323-11510delinsTA ENSP00000413239.1:n.323-11511_323-11510delinsTA
ENST00000618808.4:c.2546-11511_2546-11510delinsTA ENSP00000478868.1:n.2546-11511_2546-11510delinsTA
NM_018557.2:c.2888-11511_2888-11510delinsTA NP_061027.2:n.2888-11511_2888-11510delinsTA
XM_011511352.1:c.2999-11511_2999-11510delinsTA XP_011509654.1:n.2999-11511_2999-11510delinsTA
XM_017004341.1:c.2498-11511_2498-11510delinsTA XP_016859830.1:n.2498-11511_2498-11510delinsTA
XR_001738778.1:n.4622-11511_4622-11510delinsTA
NM_018557.3:c.2888-11511_2888-11510delinsTA MANE Select NP_061027.2:n.2888-11511_2888-11510delinsTA