Canonical Allele Identifier: CA1293294951

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038116_141038117delinsGA , CM000664.2:g.141038116_141038117delinsGA	GRCh38
NC_000002.11:g.141795685_141795686delinsGA , CM000664.1:g.141795685_141795686delinsGA	GRCh37
NC_000002.10:g.141512155_141512156delinsGA	NCBI36
NG_051023.1:g.1099347_1099348delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10869_1789+10870delinsTC MANE Select	ENSP00000374135.3:n.1789+10869_1789+10870delinsTC
ENST00000389484.7:c.1789+10869_1789+10870delinsTC	ENSP00000374135.3:n.1789+10869_1789+10870delinsTC
ENST00000434794.1:c.206-55841_206-55840delinsTC	ENSP00000413239.1:n.206-55841_206-55840delinsTC
ENST00000618808.4:c.1447+10869_1447+10870delinsTC	ENSP00000478868.1:n.1447+10869_1447+10870delinsTC
NM_018557.2:c.1789+10869_1789+10870delinsTC	NP_061027.2:n.1789+10869_1789+10870delinsTC
XM_011511352.1:c.1900+10869_1900+10870delinsTC	XP_011509654.1:n.1900+10869_1900+10870delinsTC
XM_017004341.1:c.1399+10869_1399+10870delinsTC	XP_016859830.1:n.1399+10869_1399+10870delinsTC
XR_001738778.1:n.3523+10869_3523+10870delinsTC
NM_018557.3:c.1789+10869_1789+10870delinsTC MANE Select	NP_061027.2:n.1789+10869_1789+10870delinsTC