Canonical Allele Identifier: CA1306353668

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169258946A= , CM000664.2:g.169258946A=	GRCh38
NC_000002.11:g.170115456A= , CM000664.1:g.170115456A=	GRCh37
NC_000002.10:g.169823702A=	NCBI36
NG_012634.1:g.108667T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+79T= MANE Select	ENSP00000496870.1:n.2513+79T=
ENST00000263816.7:c.2513+79T=	ENSP00000263816.3:n.2513+79T=
ENST00000443831.1:c.2102+79T=	ENSP00000409813.1:n.2102+79T=
NM_004525.2:c.2513+79T=	NP_004516.2:n.2513+79T=
XM_011511183.1:c.2513+79T=	XP_011509485.1:n.2513+79T=
XM_011511184.1:c.224+79T=	XP_011509486.1:n.224+79T=
XM_011511185.1:c.2513+79T=	XP_011509487.1:n.2513+79T=
NM_004525.3:c.2513+79T= MANE Select	NP_004516.2:n.2513+79T=
XM_011511183.3:c.2513+79T=	XP_011509485.1:n.2513+79T=
XM_011511184.2:c.224+79T=	XP_011509486.1:n.224+79T=