Canonical Allele Identifier: CA349149433
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169129065A>G , CM000664.2:g.169129065A>G GRCh38
NC_000002.11:g.169985575A>G , CM000664.1:g.169985575A>G GRCh37
NC_000002.10:g.169693821A>G NCBI36
NG_012634.1:g.238548T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13748T>C MANE Select ENSP00000496870.1:p.Phe4583Ser
ENST00000649153.1:c.4557T>C
ENST00000650252.1:c.2739T>C ENSP00000496887.1:n.2739T>C
ENST00000263816.7:c.13748T>C ENSP00000263816.3:p.Phe4583Ser
NM_004525.2:c.13748T>C NP_004516.2:p.Phe4583Ser
XM_011511183.1:c.13619T>C XP_011509485.1:p.Phe4540Ser
XM_011511184.1:c.11459T>C XP_011509486.1:p.Phe3820Ser
NM_004525.3:c.13748T>C MANE Select NP_004516.2:p.Phe4583Ser
XM_011511183.3:c.13619T>C XP_011509485.1:p.Phe4540Ser
XM_011511184.2:c.11459T>C XP_011509486.1:p.Phe3820Ser