Canonical Allele Identifier: CA1306305530
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154444_169154445delinsCA , CM000664.2:g.169154444_169154445delinsCA GRCh38
NC_000002.11:g.170010954_170010955delinsCA , CM000664.1:g.170010954_170010955delinsCA GRCh37
NC_000002.10:g.169719200_169719201delinsCA NCBI36
NG_012634.1:g.213168_213169delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+15_12295+16delinsTG MANE Select ENSP00000496870.1:n.12295+15_12295+16deli...
ENST00000649153.1:c.3195+15_3195+16delinsTG
ENST00000650252.1:c.1323+15_1323+16delinsTG ENSP00000496887.1:n.1323+15_1323+16delins...
ENST00000263816.7:c.12295+15_12295+16delinsTG ENSP00000263816.3:n.12295+15_12295+16deli...
NM_004525.2:c.12295+15_12295+16delinsTG NP_004516.2:n.12295+15_12295+16delinsTG
XM_011511183.1:c.12166+15_12166+16delinsTG XP_011509485.1:n.12166+15_12166+16delinsT...
XM_011511184.1:c.10006+15_10006+16delinsTG XP_011509486.1:n.10006+15_10006+16delinsT...
NM_004525.3:c.12295+15_12295+16delinsTG MANE Select NP_004516.2:n.12295+15_12295+16delinsTG
XM_011511183.3:c.12166+15_12166+16delinsTG XP_011509485.1:n.12166+15_12166+16delinsT...
XM_011511184.2:c.10006+15_10006+16delinsTG XP_011509486.1:n.10006+15_10006+16delinsT...