Canonical Allele Identifier: CA1306305580

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154485A= , CM000664.2:g.169154485A=	GRCh38
NC_000002.11:g.170010995A= , CM000664.1:g.170010995A=	GRCh37
NC_000002.10:g.169719241A=	NCBI36
NG_012634.1:g.213128T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12270T= MANE Select	ENSP00000496870.1:p.Asp4090=
ENST00000649153.1:c.3170T=
ENST00000650252.1:c.1298T=	ENSP00000496887.1:p.Ile433=
ENST00000263816.7:c.12270T=	ENSP00000263816.3:p.Asp4090=
NM_004525.2:c.12270T=	NP_004516.2:p.Asp4090=
XM_011511183.1:c.12141T=	XP_011509485.1:p.Asp4047=
XM_011511184.1:c.9981T=	XP_011509486.1:p.Asp3327=
NM_004525.3:c.12270T= MANE Select	NP_004516.2:p.Asp4090=
XM_011511183.3:c.12141T=	XP_011509485.1:p.Asp4047=
XM_011511184.2:c.9981T=	XP_011509486.1:p.Asp3327=