Canonical Allele Identifier: CA1293259630

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963557_140963561delinsTAAAG , CM000664.2:g.140963557_140963561delinsTAAAG	GRCh38
NC_000002.11:g.141721126_141721130delinsTAAAG , CM000664.1:g.141721126_141721130delinsTAAAG	GRCh37
NC_000002.10:g.141437596_141437600delinsTAAAG	NCBI36
NG_051023.1:g.1173903_1173907delinsCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11621_2888-11617delinsCTTTA MANE Select	ENSP00000374135.3:n.2888-11621_2888-11617delinsCTTTA
ENST00000389484.7:c.2888-11621_2888-11617delinsCTTTA	ENSP00000374135.3:n.2888-11621_2888-11617delinsCTTTA
ENST00000434794.1:c.323-11621_323-11617delinsCTTTA	ENSP00000413239.1:n.323-11621_323-11617delinsCTTTA
ENST00000618808.4:c.2546-11621_2546-11617delinsCTTTA	ENSP00000478868.1:n.2546-11621_2546-11617delinsCTTTA
NM_018557.2:c.2888-11621_2888-11617delinsCTTTA	NP_061027.2:n.2888-11621_2888-11617delinsCTTTA
XM_011511352.1:c.2999-11621_2999-11617delinsCTTTA	XP_011509654.1:n.2999-11621_2999-11617delinsCTTTA
XM_017004341.1:c.2498-11621_2498-11617delinsCTTTA	XP_016859830.1:n.2498-11621_2498-11617delinsCTTTA
XR_001738778.1:n.4622-11621_4622-11617delinsCTTTA
NM_018557.3:c.2888-11621_2888-11617delinsCTTTA MANE Select	NP_061027.2:n.2888-11621_2888-11617delinsCTTTA