Canonical Allele Identifier: CA1037173703

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696109445
• gnomAD v3: 2-140963741-AAGGTCAGGAGTTCAAGACC-A
• gnomAD v4: 2-140963741-AAGGTCAGGAGTTCAAGACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963744_140963762del , CM000664.2:g.140963744_140963762del	GRCh38
NC_000002.11:g.141721313_141721331del , CM000664.1:g.141721313_141721331del	GRCh37
NC_000002.10:g.141437783_141437801del	NCBI36
NG_051023.1:g.1173704_1173722del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11820_2888-11802del MANE Select	ENSP00000374135.3:n.2888-11820_2888-11802del
ENST00000389484.7:c.2888-11820_2888-11802del	ENSP00000374135.3:n.2888-11820_2888-11802del
ENST00000434794.1:c.323-11820_323-11802del	ENSP00000413239.1:n.323-11820_323-11802del
ENST00000618808.4:c.2546-11820_2546-11802del	ENSP00000478868.1:n.2546-11820_2546-11802del
NM_018557.2:c.2888-11820_2888-11802del	NP_061027.2:n.2888-11820_2888-11802del
XM_011511352.1:c.2999-11820_2999-11802del	XP_011509654.1:n.2999-11820_2999-11802del
XM_017004341.1:c.2498-11820_2498-11802del	XP_016859830.1:n.2498-11820_2498-11802del
XR_001738778.1:n.4622-11820_4622-11802del
NM_018557.3:c.2888-11820_2888-11802del MANE Select	NP_061027.2:n.2888-11820_2888-11802del