Canonical Allele Identifier: CA1306353982
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259570_169259571delinsAC , CM000664.2:g.169259570_169259571delinsAC GRCh38
NC_000002.11:g.170116080_170116081delinsAC , CM000664.1:g.170116080_170116081delinsAC GRCh37
NC_000002.10:g.169824326_169824327delinsAC NCBI36
NG_012634.1:g.108042_108043delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-354_2321-353delinsGT MANE Select ENSP00000496870.1:n.2321-354_2321-353delinsGT
ENST00000263816.7:c.2321-354_2321-353delinsGT ENSP00000263816.3:n.2321-354_2321-353delinsGT
ENST00000443831.1:c.1910-354_1910-353delinsGT ENSP00000409813.1:n.1910-354_1910-353delinsGT
NM_004525.2:c.2321-354_2321-353delinsGT NP_004516.2:n.2321-354_2321-353delinsGT
XM_011511183.1:c.2321-354_2321-353delinsGT XP_011509485.1:n.2321-354_2321-353delinsGT
XM_011511184.1:c.32-354_32-353delinsGT XP_011509486.1:n.32-354_32-353delinsGT
XM_011511185.1:c.2321-354_2321-353delinsGT XP_011509487.1:n.2321-354_2321-353delinsGT
NM_004525.3:c.2321-354_2321-353delinsGT MANE Select NP_004516.2:n.2321-354_2321-353delinsGT
XM_011511183.3:c.2321-354_2321-353delinsGT XP_011509485.1:n.2321-354_2321-353delinsGT
XM_011511184.2:c.32-354_32-353delinsGT XP_011509486.1:n.32-354_32-353delinsGT