Canonical Allele Identifier: CA1293259275

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696094611

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963322_140963325del , CM000664.2:g.140963322_140963325del	GRCh38
NC_000002.11:g.141720891_141720894del , CM000664.1:g.141720891_141720894del	GRCh37
NC_000002.10:g.141437361_141437364del	NCBI36
NG_051023.1:g.1174142_1174145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11382_2888-11379del MANE Select	ENSP00000374135.3:n.2888-11382_2888-11379del
ENST00000389484.7:c.2888-11382_2888-11379del	ENSP00000374135.3:n.2888-11382_2888-11379del
ENST00000434794.1:c.323-11382_323-11379del	ENSP00000413239.1:n.323-11382_323-11379del
ENST00000618808.4:c.2546-11382_2546-11379del	ENSP00000478868.1:n.2546-11382_2546-11379del
NM_018557.2:c.2888-11382_2888-11379del	NP_061027.2:n.2888-11382_2888-11379del
XM_011511352.1:c.2999-11382_2999-11379del	XP_011509654.1:n.2999-11382_2999-11379del
XM_017004341.1:c.2498-11382_2498-11379del	XP_016859830.1:n.2498-11382_2498-11379del
XR_001738778.1:n.4622-11382_4622-11379del
NM_018557.3:c.2888-11382_2888-11379del MANE Select	NP_061027.2:n.2888-11382_2888-11379del