Canonical Allele Identifier: CA1306305674

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154557T= , CM000664.2:g.169154557T=	GRCh38
NC_000002.11:g.170011067T= , CM000664.1:g.170011067T=	GRCh37
NC_000002.10:g.169719313T=	NCBI36
NG_012634.1:g.213056A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12198A= MANE Select	ENSP00000496870.1:p.Lys4066=
ENST00000649153.1:c.3098A=
ENST00000650252.1:c.1226A=	ENSP00000496887.1:p.Asn409=
ENST00000263816.7:c.12198A=	ENSP00000263816.3:p.Lys4066=
NM_004525.2:c.12198A=	NP_004516.2:p.Lys4066=
XM_011511183.1:c.12069A=	XP_011509485.1:p.Lys4023=
XM_011511184.1:c.9909A=	XP_011509486.1:p.Lys3303=
NM_004525.3:c.12198A= MANE Select	NP_004516.2:p.Lys4066=
XM_011511183.3:c.12069A=	XP_011509485.1:p.Lys4023=
XM_011511184.2:c.9909A=	XP_011509486.1:p.Lys3303=