Canonical Allele Identifier: CA1306305687

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154562G= , CM000664.2:g.169154562G=	GRCh38
NC_000002.11:g.170011072G= , CM000664.1:g.170011072G=	GRCh37
NC_000002.10:g.169719318G=	NCBI36
NG_012634.1:g.213051C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12193C= MANE Select	ENSP00000496870.1:p.Arg4065=
ENST00000649153.1:c.3093C=
ENST00000650252.1:c.1221C=	ENSP00000496887.1:p.Phe407=
ENST00000263816.7:c.12193C=	ENSP00000263816.3:p.Arg4065=
NM_004525.2:c.12193C=	NP_004516.2:p.Arg4065=
XM_011511183.1:c.12064C=	XP_011509485.1:p.Arg4022=
XM_011511184.1:c.9904C=	XP_011509486.1:p.Arg3302=
NM_004525.3:c.12193C= MANE Select	NP_004516.2:p.Arg4065=
XM_011511183.3:c.12064C=	XP_011509485.1:p.Arg4022=
XM_011511184.2:c.9904C=	XP_011509486.1:p.Arg3302=