Canonical Allele Identifier: CA2661822905
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259115_169259116insG , CM000664.2:g.169259115_169259116insG GRCh38
NC_000002.11:g.170115625_170115626insG , CM000664.1:g.170115625_170115626insG GRCh37
NC_000002.10:g.169823871_169823872insG NCBI36
NG_012634.1:g.108497_108498insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2422_2423insC MANE Select ENSP00000496870.1:p.Ile808ThrfsTer8
ENST00000263816.7:c.2422_2423insC ENSP00000263816.3:p.Ile808ThrfsTer8
ENST00000443831.1:c.2011_2012insC ENSP00000409813.1:p.Ile671ThrfsTer8
NM_004525.2:c.2422_2423insC NP_004516.2:p.Ile808ThrfsTer8
XM_011511183.1:c.2422_2423insC XP_011509485.1:p.Ile808ThrfsTer8
XM_011511184.1:c.133_134insC XP_011509486.1:p.Ile45ThrfsTer8
XM_011511185.1:c.2422_2423insC XP_011509487.1:p.Ile808ThrfsTer8
NM_004525.3:c.2422_2423insC MANE Select NP_004516.2:p.Ile808ThrfsTer8
XM_011511183.3:c.2422_2423insC XP_011509485.1:p.Ile808ThrfsTer8
XM_011511184.2:c.133_134insC XP_011509486.1:p.Ile45ThrfsTer8