Canonical Allele Identifier: CA1306353781

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259167A= , CM000664.2:g.169259167A=	GRCh38
NC_000002.11:g.170115677A= , CM000664.1:g.170115677A=	GRCh37
NC_000002.10:g.169823923A=	NCBI36
NG_012634.1:g.108446T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2371T= MANE Select	ENSP00000496870.1:p.Phe791=
ENST00000263816.7:c.2371T=	ENSP00000263816.3:p.Phe791=
ENST00000443831.1:c.1960T=	ENSP00000409813.1:p.Phe654=
NM_004525.2:c.2371T=	NP_004516.2:p.Phe791=
XM_011511183.1:c.2371T=	XP_011509485.1:p.Phe791=
XM_011511184.1:c.82T=	XP_011509486.1:p.Phe28=
XM_011511185.1:c.2371T=	XP_011509487.1:p.Phe791=
NM_004525.3:c.2371T= MANE Select	NP_004516.2:p.Phe791=
XM_011511183.3:c.2371T=	XP_011509485.1:p.Phe791=
XM_011511184.2:c.82T=	XP_011509486.1:p.Phe28=