Canonical Allele Identifier: CA2661822912
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259243_169259244insAAC , CM000664.2:g.169259243_169259244insAAC GRCh38
NC_000002.11:g.170115753_170115754insAAC , CM000664.1:g.170115753_170115754insAAC GRCh37
NC_000002.10:g.169823999_169824000insAAC NCBI36
NG_012634.1:g.108369_108370insGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2321-27_2321-26insGTT MANE Select ENSP00000496870.1:n.2321-27_2321-26insGTT...
ENST00000263816.7:c.2321-27_2321-26insGTT ENSP00000263816.3:n.2321-27_2321-26insGTT...
ENST00000443831.1:c.1910-27_1910-26insGTT ENSP00000409813.1:n.1910-27_1910-26insGTT...
NM_004525.2:c.2321-27_2321-26insGTT NP_004516.2:n.2321-27_2321-26insGTT
XM_011511183.1:c.2321-27_2321-26insGTT XP_011509485.1:n.2321-27_2321-26insGTT
XM_011511184.1:c.32-27_32-26insGTT XP_011509486.1:n.32-27_32-26insGTT
XM_011511185.1:c.2321-27_2321-26insGTT XP_011509487.1:n.2321-27_2321-26insGTT
NM_004525.3:c.2321-27_2321-26insGTT MANE Select NP_004516.2:n.2321-27_2321-26insGTT
XM_011511183.3:c.2321-27_2321-26insGTT XP_011509485.1:n.2321-27_2321-26insGTT
XM_011511184.2:c.32-27_32-26insGTT XP_011509486.1:n.32-27_32-26insGTT