Canonical Allele Identifier: CA1306305597

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154506A= , CM000664.2:g.169154506A=	GRCh38
NC_000002.11:g.170011016A= , CM000664.1:g.170011016A=	GRCh37
NC_000002.10:g.169719262A=	NCBI36
NG_012634.1:g.213107T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12249T= MANE Select	ENSP00000496870.1:p.Tyr4083=
ENST00000649153.1:c.3149T=
ENST00000650252.1:c.1277T=	ENSP00000496887.1:p.Ile426=
ENST00000263816.7:c.12249T=	ENSP00000263816.3:p.Tyr4083=
NM_004525.2:c.12249T=	NP_004516.2:p.Tyr4083=
XM_011511183.1:c.12120T=	XP_011509485.1:p.Tyr4040=
XM_011511184.1:c.9960T=	XP_011509486.1:p.Tyr3320=
NM_004525.3:c.12249T= MANE Select	NP_004516.2:p.Tyr4083=
XM_011511183.3:c.12120T=	XP_011509485.1:p.Tyr4040=
XM_011511184.2:c.9960T=	XP_011509486.1:p.Tyr3320=