Canonical Allele Identifier: CA1037180687

Gene: LRP1B

Linked Data

• gnomAD v3: 2-141037895-CTCACAT-C
• gnomAD v4: 2-141037895-CTCACAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141037896_141037901del , CM000664.2:g.141037896_141037901del	GRCh38
NC_000002.11:g.141795465_141795470del , CM000664.1:g.141795465_141795470del	GRCh37
NC_000002.10:g.141511935_141511940del	NCBI36
NG_051023.1:g.1099563_1099568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.1789+11085_1789+11090del MANE Select	ENSP00000374135.3:n.1789+11085_1789+11090del
ENST00000389484.7:c.1789+11085_1789+11090del	ENSP00000374135.3:n.1789+11085_1789+11090del
ENST00000434794.1:c.206-55625_206-55620del	ENSP00000413239.1:n.206-55625_206-55620del
ENST00000618808.4:c.1447+11085_1447+11090del	ENSP00000478868.1:n.1447+11085_1447+11090del
NM_018557.2:c.1789+11085_1789+11090del	NP_061027.2:n.1789+11085_1789+11090del
XM_011511352.1:c.1900+11085_1900+11090del	XP_011509654.1:n.1900+11085_1900+11090del
XM_017004341.1:c.1399+11085_1399+11090del	XP_016859830.1:n.1399+11085_1399+11090del
XR_001738778.1:n.3523+11085_3523+11090del
NM_018557.3:c.1789+11085_1789+11090del MANE Select	NP_061027.2:n.1789+11085_1789+11090del