Canonical Allele Identifier: CA2605192140

Gene: LRP1B

Linked Data

• gnomAD v3: 2-141038071-G-GGGCAT
• gnomAD v4: 2-141038071-G-GGGCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038072_141038076dup , CM000664.2:g.141038072_141038076dup	GRCh38
NC_000002.11:g.141795641_141795645dup , CM000664.1:g.141795641_141795645dup	GRCh37
NC_000002.10:g.141512111_141512115dup	NCBI36
NG_051023.1:g.1099388_1099392dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10910_1789+10914dup MANE Select	ENSP00000374135.3:n.1789+10910_1789+10914...
ENST00000389484.7:c.1789+10910_1789+10914dup	ENSP00000374135.3:n.1789+10910_1789+10914...
ENST00000434794.1:c.206-55800_206-55796dup	ENSP00000413239.1:n.206-55800_206-55796du...
ENST00000618808.4:c.1447+10910_1447+10914dup	ENSP00000478868.1:n.1447+10910_1447+10914...
NM_018557.2:c.1789+10910_1789+10914dup	NP_061027.2:n.1789+10910_1789+10914dup
XM_011511352.1:c.1900+10910_1900+10914dup	XP_011509654.1:n.1900+10910_1900+10914dup...
XM_017004341.1:c.1399+10910_1399+10914dup	XP_016859830.1:n.1399+10910_1399+10914dup...
XR_001738778.1:n.3523+10910_3523+10914dup
NM_018557.3:c.1789+10910_1789+10914dup MANE Select	NP_061027.2:n.1789+10910_1789+10914dup