Canonical Allele Identifier: CA1306353758
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259112C= , CM000664.2:g.169259112C= GRCh38
NC_000002.11:g.170115622C= , CM000664.1:g.170115622C= GRCh37
NC_000002.10:g.169823868C= NCBI36
NG_012634.1:g.108501G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2426G= MANE Select ENSP00000496870.1:p.Ser809=
ENST00000263816.7:c.2426G= ENSP00000263816.3:p.Ser809=
ENST00000443831.1:c.2015G= ENSP00000409813.1:p.Ser672=
NM_004525.2:c.2426G= NP_004516.2:p.Ser809=
XM_011511183.1:c.2426G= XP_011509485.1:p.Ser809=
XM_011511184.1:c.137G= XP_011509486.1:p.Ser46=
XM_011511185.1:c.2426G= XP_011509487.1:p.Ser809=
NM_004525.3:c.2426G= MANE Select NP_004516.2:p.Ser809=
XM_011511183.3:c.2426G= XP_011509485.1:p.Ser809=
XM_011511184.2:c.137G= XP_011509486.1:p.Ser46=