Canonical Allele Identifier: CA1306305607
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154511C= , CM000664.2:g.169154511C= GRCh38
NC_000002.11:g.170011021C= , CM000664.1:g.170011021C= GRCh37
NC_000002.10:g.169719267C= NCBI36
NG_012634.1:g.213102G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12244G= MANE Select ENSP00000496870.1:p.Glu4082=
ENST00000649153.1:c.3144G=
ENST00000650252.1:c.1272G= ENSP00000496887.1:p.Arg424=
ENST00000263816.7:c.12244G= ENSP00000263816.3:p.Glu4082=
NM_004525.2:c.12244G= NP_004516.2:p.Glu4082=
XM_011511183.1:c.12115G= XP_011509485.1:p.Glu4039=
XM_011511184.1:c.9955G= XP_011509486.1:p.Glu3319=
NM_004525.3:c.12244G= MANE Select NP_004516.2:p.Glu4082=
XM_011511183.3:c.12115G= XP_011509485.1:p.Glu4039=
XM_011511184.2:c.9955G= XP_011509486.1:p.Glu3319=