Canonical Allele Identifier: CA1306305423
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154296_169154297delinsCA , CM000664.2:g.169154296_169154297delinsCA GRCh38
NC_000002.11:g.170010806_170010807delinsCA , CM000664.1:g.170010806_170010807delinsCA GRCh37
NC_000002.10:g.169719052_169719053delinsCA NCBI36
NG_012634.1:g.213316_213317delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+163_12295+164delinsTG MANE Select ENSP00000496870.1:n.12295+163_12295+164de...
ENST00000649153.1:c.3195+163_3195+164delinsTG
ENST00000650252.1:c.1323+163_1323+164delinsTG ENSP00000496887.1:n.1323+163_1323+164deli...
ENST00000263816.7:c.12295+163_12295+164delinsTG ENSP00000263816.3:n.12295+163_12295+164de...
NM_004525.2:c.12295+163_12295+164delinsTG NP_004516.2:n.12295+163_12295+164delinsTG...
XM_011511183.1:c.12166+163_12166+164delinsTG XP_011509485.1:n.12166+163_12166+164delin...
XM_011511184.1:c.10006+163_10006+164delinsTG XP_011509486.1:n.10006+163_10006+164delin...
NM_004525.3:c.12295+163_12295+164delinsTG MANE Select NP_004516.2:n.12295+163_12295+164delinsTG...
XM_011511183.3:c.12166+163_12166+164delinsTG XP_011509485.1:n.12166+163_12166+164delin...
XM_011511184.2:c.10006+163_10006+164delinsTG XP_011509486.1:n.10006+163_10006+164delin...