Canonical Allele Identifier: CA1306298311

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169129060G= , CM000664.2:g.169129060G=	GRCh38
NC_000002.11:g.169985570G= , CM000664.1:g.169985570G=	GRCh37
NC_000002.10:g.169693816G=	NCBI36
NG_012634.1:g.238553C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13753C= MANE Select	ENSP00000496870.1:p.Arg4585=
ENST00000649153.1:c.4562C=
ENST00000650252.1:c.2744C=	ENSP00000496887.1:n.2744C=
ENST00000263816.7:c.13753C=	ENSP00000263816.3:p.Arg4585=
NM_004525.2:c.13753C=	NP_004516.2:p.Arg4585=
XM_011511183.1:c.13624C=	XP_011509485.1:p.Arg4542=
XM_011511184.1:c.11464C=	XP_011509486.1:p.Arg3822=
NM_004525.3:c.13753C= MANE Select	NP_004516.2:p.Arg4585=
XM_011511183.3:c.13624C=	XP_011509485.1:p.Arg4542=
XM_011511184.2:c.11464C=	XP_011509486.1:p.Arg3822=