Canonical Allele Identifier: CA1306298315
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169129071T= , CM000664.2:g.169129071T= GRCh38
NC_000002.11:g.169985581T= , CM000664.1:g.169985581T= GRCh37
NC_000002.10:g.169693827T= NCBI36
NG_012634.1:g.238542A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13742A= MANE Select ENSP00000496870.1:p.Asn4581=
ENST00000649153.1:c.4551A=
ENST00000650252.1:c.2733A= ENSP00000496887.1:n.2733A=
ENST00000263816.7:c.13742A= ENSP00000263816.3:p.Asn4581=
NM_004525.2:c.13742A= NP_004516.2:p.Asn4581=
XM_011511183.1:c.13613A= XP_011509485.1:p.Asn4538=
XM_011511184.1:c.11453A= XP_011509486.1:p.Asn3818=
NM_004525.3:c.13742A= MANE Select NP_004516.2:p.Asn4581=
XM_011511183.3:c.13613A= XP_011509485.1:p.Asn4538=
XM_011511184.2:c.11453A= XP_011509486.1:p.Asn3818=