Canonical Allele Identifier: CA1306305557
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154469T= , CM000664.2:g.169154469T= GRCh38
NC_000002.11:g.170010979T= , CM000664.1:g.170010979T= GRCh37
NC_000002.10:g.169719225T= NCBI36
NG_012634.1:g.213144A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12286A= MANE Select ENSP00000496870.1:p.Ile4096=
ENST00000649153.1:c.3186A=
ENST00000650252.1:c.1314A= ENSP00000496887.1:p.Thr438=
ENST00000263816.7:c.12286A= ENSP00000263816.3:p.Ile4096=
NM_004525.2:c.12286A= NP_004516.2:p.Ile4096=
XM_011511183.1:c.12157A= XP_011509485.1:p.Ile4053=
XM_011511184.1:c.9997A= XP_011509486.1:p.Ile3333=
NM_004525.3:c.12286A= MANE Select NP_004516.2:p.Ile4096=
XM_011511183.3:c.12157A= XP_011509485.1:p.Ile4053=
XM_011511184.2:c.9997A= XP_011509486.1:p.Ile3333=