Canonical Allele Identifier: CA1306305668

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154550G= , CM000664.2:g.169154550G=	GRCh38
NC_000002.11:g.170011060G= , CM000664.1:g.170011060G=	GRCh37
NC_000002.10:g.169719306G=	NCBI36
NG_012634.1:g.213063C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12205C= MANE Select	ENSP00000496870.1:p.Leu4069=
ENST00000649153.1:c.3105C=
ENST00000650252.1:c.1233C=	ENSP00000496887.1:p.Ile411=
ENST00000263816.7:c.12205C=	ENSP00000263816.3:p.Leu4069=
NM_004525.2:c.12205C=	NP_004516.2:p.Leu4069=
XM_011511183.1:c.12076C=	XP_011509485.1:p.Leu4026=
XM_011511184.1:c.9916C=	XP_011509486.1:p.Leu3306=
NM_004525.3:c.12205C= MANE Select	NP_004516.2:p.Leu4069=
XM_011511183.3:c.12076C=	XP_011509485.1:p.Leu4026=
XM_011511184.2:c.9916C=	XP_011509486.1:p.Leu3306=