Canonical Allele Identifier: CA1293294790

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141037957_141037958delinsAC , CM000664.2:g.141037957_141037958delinsAC	GRCh38
NC_000002.11:g.141795526_141795527delinsAC , CM000664.1:g.141795526_141795527delinsAC	GRCh37
NC_000002.10:g.141511996_141511997delinsAC	NCBI36
NG_051023.1:g.1099506_1099507delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.1789+11028_1789+11029delinsGT MANE Select	ENSP00000374135.3:n.1789+11028_1789+11029delinsGT
ENST00000389484.7:c.1789+11028_1789+11029delinsGT	ENSP00000374135.3:n.1789+11028_1789+11029delinsGT
ENST00000434794.1:c.206-55682_206-55681delinsGT	ENSP00000413239.1:n.206-55682_206-55681delinsGT
ENST00000618808.4:c.1447+11028_1447+11029delinsGT	ENSP00000478868.1:n.1447+11028_1447+11029delinsGT
NM_018557.2:c.1789+11028_1789+11029delinsGT	NP_061027.2:n.1789+11028_1789+11029delinsGT
XM_011511352.1:c.1900+11028_1900+11029delinsGT	XP_011509654.1:n.1900+11028_1900+11029delinsGT
XM_017004341.1:c.1399+11028_1399+11029delinsGT	XP_016859830.1:n.1399+11028_1399+11029delinsGT
XR_001738778.1:n.3523+11028_3523+11029delinsGT
NM_018557.3:c.1789+11028_1789+11029delinsGT MANE Select	NP_061027.2:n.1789+11028_1789+11029delinsGT