Canonical Allele Identifier: CA1293259462
Gene: LRP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963446_140963447delinsTA , CM000664.2:g.140963446_140963447delinsTA GRCh38
NC_000002.11:g.141721015_141721016delinsTA , CM000664.1:g.141721015_141721016delinsTA GRCh37
NC_000002.10:g.141437485_141437486delinsTA NCBI36
NG_051023.1:g.1174017_1174018delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11507_2888-11506delinsTA MANE Select ENSP00000374135.3:n.2888-11507_2888-11506delinsTA
ENST00000389484.7:c.2888-11507_2888-11506delinsTA ENSP00000374135.3:n.2888-11507_2888-11506delinsTA
ENST00000434794.1:c.323-11507_323-11506delinsTA ENSP00000413239.1:n.323-11507_323-11506delinsTA
ENST00000618808.4:c.2546-11507_2546-11506delinsTA ENSP00000478868.1:n.2546-11507_2546-11506delinsTA
NM_018557.2:c.2888-11507_2888-11506delinsTA NP_061027.2:n.2888-11507_2888-11506delinsTA
XM_011511352.1:c.2999-11507_2999-11506delinsTA XP_011509654.1:n.2999-11507_2999-11506delinsTA
XM_017004341.1:c.2498-11507_2498-11506delinsTA XP_016859830.1:n.2498-11507_2498-11506delinsTA
XR_001738778.1:n.4622-11507_4622-11506delinsTA
NM_018557.3:c.2888-11507_2888-11506delinsTA MANE Select NP_061027.2:n.2888-11507_2888-11506delinsTA