Canonical Allele Identifier: CA1293259172

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963259_140963261delinsGAA , CM000664.2:g.140963259_140963261delinsGAA	GRCh38
NC_000002.11:g.141720828_141720830delinsGAA , CM000664.1:g.141720828_141720830delinsGAA	GRCh37
NC_000002.10:g.141437298_141437300delinsGAA	NCBI36
NG_051023.1:g.1174203_1174205delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11321_2888-11319delinsTTC MANE Select	ENSP00000374135.3:n.2888-11321_2888-11319delinsTTC
ENST00000389484.7:c.2888-11321_2888-11319delinsTTC	ENSP00000374135.3:n.2888-11321_2888-11319delinsTTC
ENST00000434794.1:c.323-11321_323-11319delinsTTC	ENSP00000413239.1:n.323-11321_323-11319delinsTTC
ENST00000618808.4:c.2546-11321_2546-11319delinsTTC	ENSP00000478868.1:n.2546-11321_2546-11319delinsTTC
NM_018557.2:c.2888-11321_2888-11319delinsTTC	NP_061027.2:n.2888-11321_2888-11319delinsTTC
XM_011511352.1:c.2999-11321_2999-11319delinsTTC	XP_011509654.1:n.2999-11321_2999-11319delinsTTC
XM_017004341.1:c.2498-11321_2498-11319delinsTTC	XP_016859830.1:n.2498-11321_2498-11319delinsTTC
XR_001738778.1:n.4622-11321_4622-11319delinsTTC
NM_018557.3:c.2888-11321_2888-11319delinsTTC MANE Select	NP_061027.2:n.2888-11321_2888-11319delinsTTC