Canonical Allele Identifier: CA2739271565
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169196995_169196996delinsTA , CM000664.2:g.169196995_169196996delinsTA GRCh38
NC_000002.11:g.170053505_170053506delinsTA , CM000664.1:g.170053505_170053506delinsTA GRCh37
NC_000002.10:g.169761751_169761752delinsTA NCBI36
NG_012634.1:g.170617_170618delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.8613_8614delinsTA MANE Select ENSP00000496870.1:p.Ala2872Thr
ENST00000263816.7:c.8613_8614delinsTA ENSP00000263816.3:p.Ala2872Thr
NM_004525.2:c.8613_8614delinsTA NP_004516.2:p.Ala2872Thr
XM_011511183.1:c.8613_8614delinsTA XP_011509485.1:p.Ala2872Thr
XM_011511184.1:c.6324_6325delinsTA XP_011509486.1:p.Ala2109Thr
XM_011511185.1:c.8613_8614delinsTA XP_011509487.1:p.Ala2872Thr
NM_004525.3:c.8613_8614delinsTA MANE Select NP_004516.2:p.Ala2872Thr
XM_011511183.3:c.8613_8614delinsTA XP_011509485.1:p.Ala2872Thr
XM_011511184.2:c.6324_6325delinsTA XP_011509486.1:p.Ala2109Thr