Canonical Allele Identifier: CA1037180884

Gene: LRP1B

Linked Data

• gnomAD v3: 2-141038137-ATT-A
• gnomAD v4: 2-141038137-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038138_141038139del , CM000664.2:g.141038138_141038139del	GRCh38
NC_000002.11:g.141795707_141795708del , CM000664.1:g.141795707_141795708del	GRCh37
NC_000002.10:g.141512177_141512178del	NCBI36
NG_051023.1:g.1099325_1099326del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10847_1789+10848del MANE Select	ENSP00000374135.3:n.1789+10847_1789+10848del
ENST00000389484.7:c.1789+10847_1789+10848del	ENSP00000374135.3:n.1789+10847_1789+10848del
ENST00000434794.1:c.206-55863_206-55862del	ENSP00000413239.1:n.206-55863_206-55862del
ENST00000618808.4:c.1447+10847_1447+10848del	ENSP00000478868.1:n.1447+10847_1447+10848del
NM_018557.2:c.1789+10847_1789+10848del	NP_061027.2:n.1789+10847_1789+10848del
XM_011511352.1:c.1900+10847_1900+10848del	XP_011509654.1:n.1900+10847_1900+10848del
XM_017004341.1:c.1399+10847_1399+10848del	XP_016859830.1:n.1399+10847_1399+10848del
XR_001738778.1:n.3523+10847_3523+10848del
NM_018557.3:c.1789+10847_1789+10848del MANE Select	NP_061027.2:n.1789+10847_1789+10848del