Canonical Allele Identifier: CA1306349795

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247710T= , CM000664.2:g.169247710T=	GRCh38
NC_000002.11:g.170104220T= , CM000664.1:g.170104220T=	GRCh37
NC_000002.10:g.169812466T=	NCBI36
NG_012634.1:g.119903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2771-195A= MANE Select	ENSP00000496870.1:n.2771-195A=
ENST00000263816.7:c.2771-195A=	ENSP00000263816.3:n.2771-195A=
ENST00000443831.1:c.2360-195A=	ENSP00000409813.1:n.2360-195A=
NM_004525.2:c.2771-195A=	NP_004516.2:n.2771-195A=
XM_011511183.1:c.2771-195A=	XP_011509485.1:n.2771-195A=
XM_011511184.1:c.482-195A=	XP_011509486.1:n.482-195A=
XM_011511185.1:c.2771-195A=	XP_011509487.1:n.2771-195A=
NM_004525.3:c.2771-195A= MANE Select	NP_004516.2:n.2771-195A=
XM_011511183.3:c.2771-195A=	XP_011509485.1:n.2771-195A=
XM_011511184.2:c.482-195A=	XP_011509486.1:n.482-195A=