Canonical Allele Identifier: CA1306305543
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154460T= , CM000664.2:g.169154460T= GRCh38
NC_000002.11:g.170010970T= , CM000664.1:g.170010970T= GRCh37
NC_000002.10:g.169719216T= NCBI36
NG_012634.1:g.213153A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295A= MANE Select ENSP00000496870.1:p.Ser4099=
ENST00000649153.1:c.3195A=
ENST00000650252.1:c.1323A= ENSP00000496887.1:n.1323A=
ENST00000263816.7:c.12295A= ENSP00000263816.3:p.Ser4099=
NM_004525.2:c.12295A= NP_004516.2:p.Ser4099=
XM_011511183.1:c.12166A= XP_011509485.1:p.Ser4056=
XM_011511184.1:c.10006A= XP_011509486.1:p.Ser3336=
NM_004525.3:c.12295A= MANE Select NP_004516.2:p.Ser4099=
XM_011511183.3:c.12166A= XP_011509485.1:p.Ser4056=
XM_011511184.2:c.10006A= XP_011509486.1:p.Ser3336=