Canonical Allele Identifier: CA1293294961

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038122_141038123delinsTA , CM000664.2:g.141038122_141038123delinsTA	GRCh38
NC_000002.11:g.141795691_141795692delinsTA , CM000664.1:g.141795691_141795692delinsTA	GRCh37
NC_000002.10:g.141512161_141512162delinsTA	NCBI36
NG_051023.1:g.1099341_1099342delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.1789+10863_1789+10864delinsTA MANE Select	ENSP00000374135.3:n.1789+10863_1789+10864delinsTA
ENST00000389484.7:c.1789+10863_1789+10864delinsTA	ENSP00000374135.3:n.1789+10863_1789+10864delinsTA
ENST00000434794.1:c.206-55847_206-55846delinsTA	ENSP00000413239.1:n.206-55847_206-55846delinsTA
ENST00000618808.4:c.1447+10863_1447+10864delinsTA	ENSP00000478868.1:n.1447+10863_1447+10864delinsTA
NM_018557.2:c.1789+10863_1789+10864delinsTA	NP_061027.2:n.1789+10863_1789+10864delinsTA
XM_011511352.1:c.1900+10863_1900+10864delinsTA	XP_011509654.1:n.1900+10863_1900+10864delinsTA
XM_017004341.1:c.1399+10863_1399+10864delinsTA	XP_016859830.1:n.1399+10863_1399+10864delinsTA
XR_001738778.1:n.3523+10863_3523+10864delinsTA
NM_018557.3:c.1789+10863_1789+10864delinsTA MANE Select	NP_061027.2:n.1789+10863_1789+10864delinsTA