Canonical Allele Identifier: CA1306349629
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247351_169247354delinsTAAA , CM000664.2:g.169247351_169247354delinsTAAA GRCh38
NC_000002.11:g.170103861_170103864delinsTAAA , CM000664.1:g.170103861_170103864delinsTAAA GRCh37
NC_000002.10:g.169812107_169812110delinsTAAA NCBI36
NG_012634.1:g.120259_120262delinsTTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2908+24_2908+27delinsTTTA MANE Select ENSP00000496870.1:n.2908+24_2908+27delins...
ENST00000263816.7:c.2908+24_2908+27delinsTTTA ENSP00000263816.3:n.2908+24_2908+27delins...
ENST00000443831.1:c.2497+24_2497+27delinsTTTA ENSP00000409813.1:n.2497+24_2497+27delins...
NM_004525.2:c.2908+24_2908+27delinsTTTA NP_004516.2:n.2908+24_2908+27delinsTTTA
XM_011511183.1:c.2908+24_2908+27delinsTTTA XP_011509485.1:n.2908+24_2908+27delinsTTT...
XM_011511184.1:c.619+24_619+27delinsTTTA XP_011509486.1:n.619+24_619+27delinsTTTA
XM_011511185.1:c.2908+24_2908+27delinsTTTA XP_011509487.1:n.2908+24_2908+27delinsTTT...
NM_004525.3:c.2908+24_2908+27delinsTTTA MANE Select NP_004516.2:n.2908+24_2908+27delinsTTTA
XM_011511183.3:c.2908+24_2908+27delinsTTTA XP_011509485.1:n.2908+24_2908+27delinsTTT...
XM_011511184.2:c.619+24_619+27delinsTTTA XP_011509486.1:n.619+24_619+27delinsTTTA