Canonical Allele Identifier: CA1293259003

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963105_140963106delinsTA , CM000664.2:g.140963105_140963106delinsTA	GRCh38
NC_000002.11:g.141720674_141720675delinsTA , CM000664.1:g.141720674_141720675delinsTA	GRCh37
NC_000002.10:g.141437144_141437145delinsTA	NCBI36
NG_051023.1:g.1174358_1174359delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11166_2888-11165delinsTA MANE Select	ENSP00000374135.3:n.2888-11166_2888-11165delinsTA
ENST00000389484.7:c.2888-11166_2888-11165delinsTA	ENSP00000374135.3:n.2888-11166_2888-11165delinsTA
ENST00000434794.1:c.323-11166_323-11165delinsTA	ENSP00000413239.1:n.323-11166_323-11165delinsTA
ENST00000618808.4:c.2546-11166_2546-11165delinsTA	ENSP00000478868.1:n.2546-11166_2546-11165delinsTA
NM_018557.2:c.2888-11166_2888-11165delinsTA	NP_061027.2:n.2888-11166_2888-11165delinsTA
XM_011511352.1:c.2999-11166_2999-11165delinsTA	XP_011509654.1:n.2999-11166_2999-11165delinsTA
XM_017004341.1:c.2498-11166_2498-11165delinsTA	XP_016859830.1:n.2498-11166_2498-11165delinsTA
XR_001738778.1:n.4622-11166_4622-11165delinsTA
NM_018557.3:c.2888-11166_2888-11165delinsTA MANE Select	NP_061027.2:n.2888-11166_2888-11165delinsTA