Canonical Allele Identifier: CA1306353785

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259178T= , CM000664.2:g.169259178T=	GRCh38
NC_000002.11:g.170115688T= , CM000664.1:g.170115688T=	GRCh37
NC_000002.10:g.169823934T=	NCBI36
NG_012634.1:g.108435A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2360A= MANE Select	ENSP00000496870.1:p.Glu787=
ENST00000263816.7:c.2360A=	ENSP00000263816.3:p.Glu787=
ENST00000443831.1:c.1949A=	ENSP00000409813.1:p.Glu650=
NM_004525.2:c.2360A=	NP_004516.2:p.Glu787=
XM_011511183.1:c.2360A=	XP_011509485.1:p.Glu787=
XM_011511184.1:c.71A=	XP_011509486.1:p.Glu24=
XM_011511185.1:c.2360A=	XP_011509487.1:p.Glu787=
NM_004525.3:c.2360A= MANE Select	NP_004516.2:p.Glu787=
XM_011511183.3:c.2360A=	XP_011509485.1:p.Glu787=
XM_011511184.2:c.71A=	XP_011509486.1:p.Glu24=