Canonical Allele Identifier: CA1306353841
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259307_169259311delinsGAGTT , CM000664.2:g.169259307_169259311delinsGAGTT GRCh38
NC_000002.11:g.170115817_170115821delinsGAGTT , CM000664.1:g.170115817_170115821delinsGAGTT GRCh37
NC_000002.10:g.169824063_169824067delinsGAGTT NCBI36
NG_012634.1:g.108302_108306delinsAACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2321-94_2321-90delinsAACTC MANE Select ENSP00000496870.1:n.2321-94_2321-90delinsAACTC
ENST00000263816.7:c.2321-94_2321-90delinsAACTC ENSP00000263816.3:n.2321-94_2321-90delinsAACTC
ENST00000443831.1:c.1910-94_1910-90delinsAACTC ENSP00000409813.1:n.1910-94_1910-90delinsAACTC
NM_004525.2:c.2321-94_2321-90delinsAACTC NP_004516.2:n.2321-94_2321-90delinsAACTC
XM_011511183.1:c.2321-94_2321-90delinsAACTC XP_011509485.1:n.2321-94_2321-90delinsAACTC
XM_011511184.1:c.32-94_32-90delinsAACTC XP_011509486.1:n.32-94_32-90delinsAACTC
XM_011511185.1:c.2321-94_2321-90delinsAACTC XP_011509487.1:n.2321-94_2321-90delinsAACTC
NM_004525.3:c.2321-94_2321-90delinsAACTC MANE Select NP_004516.2:n.2321-94_2321-90delinsAACTC
XM_011511183.3:c.2321-94_2321-90delinsAACTC XP_011509485.1:n.2321-94_2321-90delinsAACTC
XM_011511184.2:c.32-94_32-90delinsAACTC XP_011509486.1:n.32-94_32-90delinsAACTC