Canonical Allele Identifier: CA1306298312
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169129063T= , CM000664.2:g.169129063T= GRCh38
NC_000002.11:g.169985573T= , CM000664.1:g.169985573T= GRCh37
NC_000002.10:g.169693819T= NCBI36
NG_012634.1:g.238550A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13750A= MANE Select ENSP00000496870.1:p.Lys4584=
ENST00000649153.1:c.4559A=
ENST00000650252.1:c.2741A= ENSP00000496887.1:n.2741A=
ENST00000263816.7:c.13750A= ENSP00000263816.3:p.Lys4584=
NM_004525.2:c.13750A= NP_004516.2:p.Lys4584=
XM_011511183.1:c.13621A= XP_011509485.1:p.Lys4541=
XM_011511184.1:c.11461A= XP_011509486.1:p.Lys3821=
NM_004525.3:c.13750A= MANE Select NP_004516.2:p.Lys4584=
XM_011511183.3:c.13621A= XP_011509485.1:p.Lys4541=
XM_011511184.2:c.11461A= XP_011509486.1:p.Lys3821=