Canonical Allele Identifier: CA1306305506
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154412C= , CM000664.2:g.169154412C= GRCh38
NC_000002.11:g.170010922C= , CM000664.1:g.170010922C= GRCh37
NC_000002.10:g.169719168C= NCBI36
NG_012634.1:g.213201G=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+48G= MANE Select ENSP00000496870.1:n.12295+48G=
ENST00000649153.1:c.3195+48G=
ENST00000650252.1:c.1323+48G= ENSP00000496887.1:n.1323+48G=
ENST00000263816.7:c.12295+48G= ENSP00000263816.3:n.12295+48G=
NM_004525.2:c.12295+48G= NP_004516.2:n.12295+48G=
XM_011511183.1:c.12166+48G= XP_011509485.1:n.12166+48G=
XM_011511184.1:c.10006+48G= XP_011509486.1:n.10006+48G=
NM_004525.3:c.12295+48G= MANE Select NP_004516.2:n.12295+48G=
XM_011511183.3:c.12166+48G= XP_011509485.1:n.12166+48G=
XM_011511184.2:c.10006+48G= XP_011509486.1:n.10006+48G=