Canonical Allele Identifier: CA1306305578

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154476G= , CM000664.2:g.169154476G=	GRCh38
NC_000002.11:g.170010986G= , CM000664.1:g.170010986G=	GRCh37
NC_000002.10:g.169719232G=	NCBI36
NG_012634.1:g.213137C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12279C= MANE Select	ENSP00000496870.1:p.Pro4093=
ENST00000649153.1:c.3179C=
ENST00000650252.1:c.1307C=	ENSP00000496887.1:p.Pro436=
ENST00000263816.7:c.12279C=	ENSP00000263816.3:p.Pro4093=
NM_004525.2:c.12279C=	NP_004516.2:p.Pro4093=
XM_011511183.1:c.12150C=	XP_011509485.1:p.Pro4050=
XM_011511184.1:c.9990C=	XP_011509486.1:p.Pro3330=
NM_004525.3:c.12279C= MANE Select	NP_004516.2:p.Pro4093=
XM_011511183.3:c.12150C=	XP_011509485.1:p.Pro4050=
XM_011511184.2:c.9990C=	XP_011509486.1:p.Pro3330=