Canonical Allele Identifier: CA1306305662

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154539C= , CM000664.2:g.169154539C=	GRCh38
NC_000002.11:g.170011049C= , CM000664.1:g.170011049C=	GRCh37
NC_000002.10:g.169719295C=	NCBI36
NG_012634.1:g.213074G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12216G= MANE Select	ENSP00000496870.1:p.Glu4072=
ENST00000649153.1:c.3116G=
ENST00000650252.1:c.1244G=	ENSP00000496887.1:p.Arg415=
ENST00000263816.7:c.12216G=	ENSP00000263816.3:p.Glu4072=
NM_004525.2:c.12216G=	NP_004516.2:p.Glu4072=
XM_011511183.1:c.12087G=	XP_011509485.1:p.Glu4029=
XM_011511184.1:c.9927G=	XP_011509486.1:p.Glu3309=
NM_004525.3:c.12216G= MANE Select	NP_004516.2:p.Glu4072=
XM_011511183.3:c.12087G=	XP_011509485.1:p.Glu4029=
XM_011511184.2:c.9927G=	XP_011509486.1:p.Glu3309=