Canonical Allele Identifier: CA1306305402

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154269A= , CM000664.2:g.169154269A=	GRCh38
NC_000002.11:g.170010779A= , CM000664.1:g.170010779A=	GRCh37
NC_000002.10:g.169719025A=	NCBI36
NG_012634.1:g.213344T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+191T= MANE Select	ENSP00000496870.1:n.12295+191T=
ENST00000649153.1:c.3195+191T=
ENST00000650252.1:c.1323+191T=	ENSP00000496887.1:n.1323+191T=
ENST00000263816.7:c.12295+191T=	ENSP00000263816.3:n.12295+191T=
NM_004525.2:c.12295+191T=	NP_004516.2:n.12295+191T=
XM_011511183.1:c.12166+191T=	XP_011509485.1:n.12166+191T=
XM_011511184.1:c.10006+191T=	XP_011509486.1:n.10006+191T=
NM_004525.3:c.12295+191T= MANE Select	NP_004516.2:n.12295+191T=
XM_011511183.3:c.12166+191T=	XP_011509485.1:n.12166+191T=
XM_011511184.2:c.10006+191T=	XP_011509486.1:n.10006+191T=