Canonical Allele Identifier: CA1293259437

Gene: LRP1B

Linked Data

• dbSNP Id: rs140209072

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963457_140963460dup , CM000664.2:g.140963457_140963460dup	GRCh38
NC_000002.11:g.141721026_141721029dup , CM000664.1:g.141721026_141721029dup	GRCh37
NC_000002.10:g.141437496_141437499dup	NCBI36
NG_051023.1:g.1174017_1174020dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11507_2888-11504dup MANE Select	ENSP00000374135.3:n.2888-11507_2888-11504dup
ENST00000389484.7:c.2888-11507_2888-11504dup	ENSP00000374135.3:n.2888-11507_2888-11504dup
ENST00000434794.1:c.323-11507_323-11504dup	ENSP00000413239.1:n.323-11507_323-11504dup
ENST00000618808.4:c.2546-11507_2546-11504dup	ENSP00000478868.1:n.2546-11507_2546-11504dup
NM_018557.2:c.2888-11507_2888-11504dup	NP_061027.2:n.2888-11507_2888-11504dup
XM_011511352.1:c.2999-11507_2999-11504dup	XP_011509654.1:n.2999-11507_2999-11504dup
XM_017004341.1:c.2498-11507_2498-11504dup	XP_016859830.1:n.2498-11507_2498-11504dup
XR_001738778.1:n.4622-11507_4622-11504dup
NM_018557.3:c.2888-11507_2888-11504dup MANE Select	NP_061027.2:n.2888-11507_2888-11504dup