Canonical Allele Identifier: CA2661822904
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259111_169259112insAGAGTATCAGTGTCATGAGGCTAG , CM000664.2:g.169259111_169259112insAGAGTATCAGTGTCATGAGGCTAG GRCh38
NC_000002.11:g.170115621_170115622insAGAGTATCAGTGTCATGAGGCTAG , CM000664.1:g.170115621_170115622insAGAGTATCAGTGTCATGAGGCTAG GRCh37
NC_000002.10:g.169823867_169823868insAGAGTATCAGTGTCATGAGGCTAG NCBI36
NG_012634.1:g.108501_108502insCTAGCCTCATGACACTGATACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2426_2427insCTAGCCTCATGACACTGATACTCT MANE Select ENSP00000496870.1:p.Ser810Ter
ENST00000263816.7:c.2426_2427insCTAGCCTCATGACACTGATACTCT ENSP00000263816.3:p.Ser810Ter
ENST00000443831.1:c.2015_2016insCTAGCCTCATGACACTGATACTCT ENSP00000409813.1:p.Ser673Ter
NM_004525.2:c.2426_2427insCTAGCCTCATGACACTGATACTCT NP_004516.2:p.Ser810Ter
XM_011511183.1:c.2426_2427insCTAGCCTCATGACACTGATACTCT XP_011509485.1:p.Ser810Ter
XM_011511184.1:c.137_138insCTAGCCTCATGACACTGATACTCT XP_011509486.1:p.Ser47Ter
XM_011511185.1:c.2426_2427insCTAGCCTCATGACACTGATACTCT XP_011509487.1:p.Ser810Ter
NM_004525.3:c.2426_2427insCTAGCCTCATGACACTGATACTCT MANE Select NP_004516.2:p.Ser810Ter
XM_011511183.3:c.2426_2427insCTAGCCTCATGACACTGATACTCT XP_011509485.1:p.Ser810Ter
XM_011511184.2:c.137_138insCTAGCCTCATGACACTGATACTCT XP_011509486.1:p.Ser47Ter