Canonical Allele Identifier: CA1293294979

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038135_141038137delinsTAA , CM000664.2:g.141038135_141038137delinsTAA	GRCh38
NC_000002.11:g.141795704_141795706delinsTAA , CM000664.1:g.141795704_141795706delinsTAA	GRCh37
NC_000002.10:g.141512174_141512176delinsTAA	NCBI36
NG_051023.1:g.1099327_1099329delinsTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10849_1789+10851delinsTTA MANE Select	ENSP00000374135.3:n.1789+10849_1789+10851delinsTTA
ENST00000389484.7:c.1789+10849_1789+10851delinsTTA	ENSP00000374135.3:n.1789+10849_1789+10851delinsTTA
ENST00000434794.1:c.206-55861_206-55859delinsTTA	ENSP00000413239.1:n.206-55861_206-55859delinsTTA
ENST00000618808.4:c.1447+10849_1447+10851delinsTTA	ENSP00000478868.1:n.1447+10849_1447+10851delinsTTA
NM_018557.2:c.1789+10849_1789+10851delinsTTA	NP_061027.2:n.1789+10849_1789+10851delinsTTA
XM_011511352.1:c.1900+10849_1900+10851delinsTTA	XP_011509654.1:n.1900+10849_1900+10851delinsTTA
XM_017004341.1:c.1399+10849_1399+10851delinsTTA	XP_016859830.1:n.1399+10849_1399+10851delinsTTA
XR_001738778.1:n.3523+10849_3523+10851delinsTTA
NM_018557.3:c.1789+10849_1789+10851delinsTTA MANE Select	NP_061027.2:n.1789+10849_1789+10851delinsTTA