Canonical Allele Identifier: CA1306305659

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154537C= , CM000664.2:g.169154537C=	GRCh38
NC_000002.11:g.170011047C= , CM000664.1:g.170011047C=	GRCh37
NC_000002.10:g.169719293C=	NCBI36
NG_012634.1:g.213076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12218G= MANE Select	ENSP00000496870.1:p.Arg4073=
ENST00000649153.1:c.3118G=
ENST00000650252.1:c.1246G=	ENSP00000496887.1:p.Gly416=
ENST00000263816.7:c.12218G=	ENSP00000263816.3:p.Arg4073=
NM_004525.2:c.12218G=	NP_004516.2:p.Arg4073=
XM_011511183.1:c.12089G=	XP_011509485.1:p.Arg4030=
XM_011511184.1:c.9929G=	XP_011509486.1:p.Arg3310=
NM_004525.3:c.12218G= MANE Select	NP_004516.2:p.Arg4073=
XM_011511183.3:c.12089G=	XP_011509485.1:p.Arg4030=
XM_011511184.2:c.9929G=	XP_011509486.1:p.Arg3310=