Canonical Allele Identifier: CA1306305562

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154471T= , CM000664.2:g.169154471T=	GRCh38
NC_000002.11:g.170010981T= , CM000664.1:g.170010981T=	GRCh37
NC_000002.10:g.169719227T=	NCBI36
NG_012634.1:g.213142A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12284A= MANE Select	ENSP00000496870.1:p.Asp4095=
ENST00000649153.1:c.3184A=
ENST00000650252.1:c.1312A=	ENSP00000496887.1:p.Thr438=
ENST00000263816.7:c.12284A=	ENSP00000263816.3:p.Asp4095=
NM_004525.2:c.12284A=	NP_004516.2:p.Asp4095=
XM_011511183.1:c.12155A=	XP_011509485.1:p.Asp4052=
XM_011511184.1:c.9995A=	XP_011509486.1:p.Asp3332=
NM_004525.3:c.12284A= MANE Select	NP_004516.2:p.Asp4095=
XM_011511183.3:c.12155A=	XP_011509485.1:p.Asp4052=
XM_011511184.2:c.9995A=	XP_011509486.1:p.Asp3332=