Canonical Allele Identifier: CA1293259239

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696093246

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963285_140963289del , CM000664.2:g.140963285_140963289del	GRCh38
NC_000002.11:g.141720854_141720858del , CM000664.1:g.141720854_141720858del	GRCh37
NC_000002.10:g.141437324_141437328del	NCBI36
NG_051023.1:g.1174175_1174179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11349_2888-11345del MANE Select	ENSP00000374135.3:n.2888-11349_2888-11345del
ENST00000389484.7:c.2888-11349_2888-11345del	ENSP00000374135.3:n.2888-11349_2888-11345del
ENST00000434794.1:c.323-11349_323-11345del	ENSP00000413239.1:n.323-11349_323-11345del
ENST00000618808.4:c.2546-11349_2546-11345del	ENSP00000478868.1:n.2546-11349_2546-11345del
NM_018557.2:c.2888-11349_2888-11345del	NP_061027.2:n.2888-11349_2888-11345del
XM_011511352.1:c.2999-11349_2999-11345del	XP_011509654.1:n.2999-11349_2999-11345del
XM_017004341.1:c.2498-11349_2498-11345del	XP_016859830.1:n.2498-11349_2498-11345del
XR_001738778.1:n.4622-11349_4622-11345del
NM_018557.3:c.2888-11349_2888-11345del MANE Select	NP_061027.2:n.2888-11349_2888-11345del