Canonical Allele Identifier: CA1306305393

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154254G= , CM000664.2:g.169154254G=	GRCh38
NC_000002.11:g.170010764G= , CM000664.1:g.170010764G=	GRCh37
NC_000002.10:g.169719010G=	NCBI36
NG_012634.1:g.213359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+206C= MANE Select	ENSP00000496870.1:n.12295+206C=
ENST00000649153.1:c.3195+206C=
ENST00000650252.1:c.1323+206C=	ENSP00000496887.1:n.1323+206C=
ENST00000263816.7:c.12295+206C=	ENSP00000263816.3:n.12295+206C=
NM_004525.2:c.12295+206C=	NP_004516.2:n.12295+206C=
XM_011511183.1:c.12166+206C=	XP_011509485.1:n.12166+206C=
XM_011511184.1:c.10006+206C=	XP_011509486.1:n.10006+206C=
NM_004525.3:c.12295+206C= MANE Select	NP_004516.2:n.12295+206C=
XM_011511183.3:c.12166+206C=	XP_011509485.1:n.12166+206C=
XM_011511184.2:c.10006+206C=	XP_011509486.1:n.10006+206C=