Canonical Allele Identifier: CA1306353735
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259063_169259064delinsTA , CM000664.2:g.169259063_169259064delinsTA GRCh38
NC_000002.11:g.170115573_170115574delinsTA , CM000664.1:g.170115573_170115574delinsTA GRCh37
NC_000002.10:g.169823819_169823820delinsTA NCBI36
NG_012634.1:g.108549_108550delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2474_2475delinsTA MANE Select ENSP00000496870.1:p.Leu825=
ENST00000263816.7:c.2474_2475delinsTA ENSP00000263816.3:p.Leu825=
ENST00000443831.1:c.2063_2064delinsTA ENSP00000409813.1:p.Leu688=
NM_004525.2:c.2474_2475delinsTA NP_004516.2:p.Leu825=
XM_011511183.1:c.2474_2475delinsTA XP_011509485.1:p.Leu825=
XM_011511184.1:c.185_186delinsTA XP_011509486.1:p.Leu62=
XM_011511185.1:c.2474_2475delinsTA XP_011509487.1:p.Leu825=
NM_004525.3:c.2474_2475delinsTA MANE Select NP_004516.2:p.Leu825=
XM_011511183.3:c.2474_2475delinsTA XP_011509485.1:p.Leu825=
XM_011511184.2:c.185_186delinsTA XP_011509486.1:p.Leu62=