Canonical Allele Identifier: CA1306305391

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154253C= , CM000664.2:g.169154253C=	GRCh38
NC_000002.11:g.170010763C= , CM000664.1:g.170010763C=	GRCh37
NC_000002.10:g.169719009C=	NCBI36
NG_012634.1:g.213360G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+207G= MANE Select	ENSP00000496870.1:n.12295+207G=
ENST00000649153.1:c.3195+207G=
ENST00000650252.1:c.1323+207G=	ENSP00000496887.1:n.1323+207G=
ENST00000263816.7:c.12295+207G=	ENSP00000263816.3:n.12295+207G=
NM_004525.2:c.12295+207G=	NP_004516.2:n.12295+207G=
XM_011511183.1:c.12166+207G=	XP_011509485.1:n.12166+207G=
XM_011511184.1:c.10006+207G=	XP_011509486.1:n.10006+207G=
NM_004525.3:c.12295+207G= MANE Select	NP_004516.2:n.12295+207G=
XM_011511183.3:c.12166+207G=	XP_011509485.1:n.12166+207G=
XM_011511184.2:c.10006+207G=	XP_011509486.1:n.10006+207G=