Canonical Allele Identifier: CA1293259276

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963320_140963321delinsAG , CM000664.2:g.140963320_140963321delinsAG	GRCh38
NC_000002.11:g.141720889_141720890delinsAG , CM000664.1:g.141720889_141720890delinsAG	GRCh37
NC_000002.10:g.141437359_141437360delinsAG	NCBI36
NG_051023.1:g.1174143_1174144delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11381_2888-11380delinsCT MANE Select	ENSP00000374135.3:n.2888-11381_2888-11380delinsCT
ENST00000389484.7:c.2888-11381_2888-11380delinsCT	ENSP00000374135.3:n.2888-11381_2888-11380delinsCT
ENST00000434794.1:c.323-11381_323-11380delinsCT	ENSP00000413239.1:n.323-11381_323-11380delinsCT
ENST00000618808.4:c.2546-11381_2546-11380delinsCT	ENSP00000478868.1:n.2546-11381_2546-11380delinsCT
NM_018557.2:c.2888-11381_2888-11380delinsCT	NP_061027.2:n.2888-11381_2888-11380delinsCT
XM_011511352.1:c.2999-11381_2999-11380delinsCT	XP_011509654.1:n.2999-11381_2999-11380delinsCT
XM_017004341.1:c.2498-11381_2498-11380delinsCT	XP_016859830.1:n.2498-11381_2498-11380delinsCT
XR_001738778.1:n.4622-11381_4622-11380delinsCT
NM_018557.3:c.2888-11381_2888-11380delinsCT MANE Select	NP_061027.2:n.2888-11381_2888-11380delinsCT