Canonical Allele Identifier: CA1306305569
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154473C= , CM000664.2:g.169154473C= GRCh38
NC_000002.11:g.170010983C= , CM000664.1:g.170010983C= GRCh37
NC_000002.10:g.169719229C= NCBI36
NG_012634.1:g.213140G=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12282G= MANE Select ENSP00000496870.1:p.Lys4094=
ENST00000649153.1:c.3182G=
ENST00000650252.1:c.1310G= ENSP00000496887.1:p.Arg437=
ENST00000263816.7:c.12282G= ENSP00000263816.3:p.Lys4094=
NM_004525.2:c.12282G= NP_004516.2:p.Lys4094=
XM_011511183.1:c.12153G= XP_011509485.1:p.Lys4051=
XM_011511184.1:c.9993G= XP_011509486.1:p.Lys3331=
NM_004525.3:c.12282G= MANE Select NP_004516.2:p.Lys4094=
XM_011511183.3:c.12153G= XP_011509485.1:p.Lys4051=
XM_011511184.2:c.9993G= XP_011509486.1:p.Lys3331=