Canonical Allele Identifier: CA1306305545
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154464G= , CM000664.2:g.169154464G= GRCh38
NC_000002.11:g.170010974G= , CM000664.1:g.170010974G= GRCh37
NC_000002.10:g.169719220G= NCBI36
NG_012634.1:g.213149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.12291C= MANE Select ENSP00000496870.1:p.Gly4097=
ENST00000649153.1:c.3191C=
ENST00000650252.1:c.1319C= ENSP00000496887.1:n.1319C=
ENST00000263816.7:c.12291C= ENSP00000263816.3:p.Gly4097=
NM_004525.2:c.12291C= NP_004516.2:p.Gly4097=
XM_011511183.1:c.12162C= XP_011509485.1:p.Gly4054=
XM_011511184.1:c.10002C= XP_011509486.1:p.Gly3334=
NM_004525.3:c.12291C= MANE Select NP_004516.2:p.Gly4097=
XM_011511183.3:c.12162C= XP_011509485.1:p.Gly4054=
XM_011511184.2:c.10002C= XP_011509486.1:p.Gly3334=