Canonical Allele Identifier: CA1306305779

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154626T= , CM000664.2:g.169154626T=	GRCh38
NC_000002.11:g.170011136T= , CM000664.1:g.170011136T=	GRCh37
NC_000002.10:g.169719382T=	NCBI36
NG_012634.1:g.212987A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12152-23A= MANE Select	ENSP00000496870.1:n.12152-23A=
ENST00000649153.1:c.3052-23A=
ENST00000650252.1:c.1184-27A=	ENSP00000496887.1:n.1184-27A=
ENST00000263816.7:c.12152-23A=	ENSP00000263816.3:n.12152-23A=
NM_004525.2:c.12152-23A=	NP_004516.2:n.12152-23A=
XM_011511183.1:c.12023-23A=	XP_011509485.1:n.12023-23A=
XM_011511184.1:c.9863-23A=	XP_011509486.1:n.9863-23A=
NM_004525.3:c.12152-23A= MANE Select	NP_004516.2:n.12152-23A=
XM_011511183.3:c.12023-23A=	XP_011509485.1:n.12023-23A=
XM_011511184.2:c.9863-23A=	XP_011509486.1:n.9863-23A=