Canonical Allele Identifier: CA1306305522
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154438_169154439delinsAG , CM000664.2:g.169154438_169154439delinsAG GRCh38
NC_000002.11:g.170010948_170010949delinsAG , CM000664.1:g.170010948_170010949delinsAG GRCh37
NC_000002.10:g.169719194_169719195delinsAG NCBI36
NG_012634.1:g.213174_213175delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+21_12295+22delinsCT MANE Select ENSP00000496870.1:n.12295+21_12295+22deli...
ENST00000649153.1:c.3195+21_3195+22delinsCT
ENST00000650252.1:c.1323+21_1323+22delinsCT ENSP00000496887.1:n.1323+21_1323+22delins...
ENST00000263816.7:c.12295+21_12295+22delinsCT ENSP00000263816.3:n.12295+21_12295+22deli...
NM_004525.2:c.12295+21_12295+22delinsCT NP_004516.2:n.12295+21_12295+22delinsCT
XM_011511183.1:c.12166+21_12166+22delinsCT XP_011509485.1:n.12166+21_12166+22delinsC...
XM_011511184.1:c.10006+21_10006+22delinsCT XP_011509486.1:n.10006+21_10006+22delinsC...
NM_004525.3:c.12295+21_12295+22delinsCT MANE Select NP_004516.2:n.12295+21_12295+22delinsCT
XM_011511183.3:c.12166+21_12166+22delinsCT XP_011509485.1:n.12166+21_12166+22delinsC...
XM_011511184.2:c.10006+21_10006+22delinsCT XP_011509486.1:n.10006+21_10006+22delinsC...