Canonical Allele Identifier: CA1293259167

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963258_140963259delinsTG , CM000664.2:g.140963258_140963259delinsTG	GRCh38
NC_000002.11:g.141720827_141720828delinsTG , CM000664.1:g.141720827_141720828delinsTG	GRCh37
NC_000002.10:g.141437297_141437298delinsTG	NCBI36
NG_051023.1:g.1174205_1174206delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11319_2888-11318delinsCA MANE Select	ENSP00000374135.3:n.2888-11319_2888-11318delinsCA
ENST00000389484.7:c.2888-11319_2888-11318delinsCA	ENSP00000374135.3:n.2888-11319_2888-11318delinsCA
ENST00000434794.1:c.323-11319_323-11318delinsCA	ENSP00000413239.1:n.323-11319_323-11318delinsCA
ENST00000618808.4:c.2546-11319_2546-11318delinsCA	ENSP00000478868.1:n.2546-11319_2546-11318delinsCA
NM_018557.2:c.2888-11319_2888-11318delinsCA	NP_061027.2:n.2888-11319_2888-11318delinsCA
XM_011511352.1:c.2999-11319_2999-11318delinsCA	XP_011509654.1:n.2999-11319_2999-11318delinsCA
XM_017004341.1:c.2498-11319_2498-11318delinsCA	XP_016859830.1:n.2498-11319_2498-11318delinsCA
XR_001738778.1:n.4622-11319_4622-11318delinsCA
NM_018557.3:c.2888-11319_2888-11318delinsCA MANE Select	NP_061027.2:n.2888-11319_2888-11318delinsCA