Canonical Allele Identifier: CA1306353753
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259106A= , CM000664.2:g.169259106A= GRCh38
NC_000002.11:g.170115616A= , CM000664.1:g.170115616A= GRCh37
NC_000002.10:g.169823862A= NCBI36
NG_012634.1:g.108507T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2432T= MANE Select ENSP00000496870.1:p.Met811=
ENST00000263816.7:c.2432T= ENSP00000263816.3:p.Met811=
ENST00000443831.1:c.2021T= ENSP00000409813.1:p.Met674=
NM_004525.2:c.2432T= NP_004516.2:p.Met811=
XM_011511183.1:c.2432T= XP_011509485.1:p.Met811=
XM_011511184.1:c.143T= XP_011509486.1:p.Met48=
XM_011511185.1:c.2432T= XP_011509487.1:p.Met811=
NM_004525.3:c.2432T= MANE Select NP_004516.2:p.Met811=
XM_011511183.3:c.2432T= XP_011509485.1:p.Met811=
XM_011511184.2:c.143T= XP_011509486.1:p.Met48=