Canonical Allele Identifier: CA1306305573

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154475T= , CM000664.2:g.169154475T=	GRCh38
NC_000002.11:g.170010985T= , CM000664.1:g.170010985T=	GRCh37
NC_000002.10:g.169719231T=	NCBI36
NG_012634.1:g.213138A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12280A= MANE Select	ENSP00000496870.1:p.Lys4094=
ENST00000649153.1:c.3180A=
ENST00000650252.1:c.1308A=	ENSP00000496887.1:p.Pro436=
ENST00000263816.7:c.12280A=	ENSP00000263816.3:p.Lys4094=
NM_004525.2:c.12280A=	NP_004516.2:p.Lys4094=
XM_011511183.1:c.12151A=	XP_011509485.1:p.Lys4051=
XM_011511184.1:c.9991A=	XP_011509486.1:p.Lys3331=
NM_004525.3:c.12280A= MANE Select	NP_004516.2:p.Lys4094=
XM_011511183.3:c.12151A=	XP_011509485.1:p.Lys4051=
XM_011511184.2:c.9991A=	XP_011509486.1:p.Lys3331=