Canonical Allele Identifier: CA2753102829

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259447_169259448insCA , CM000664.2:g.169259447_169259448insCA	GRCh38
NC_000002.11:g.170115957_170115958insCA , CM000664.1:g.170115957_170115958insCA	GRCh37
NC_000002.10:g.169824203_169824204insCA	NCBI36
NG_012634.1:g.108166_108167insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-230_2321-229insGT MANE Select	ENSP00000496870.1:n.2321-230_2321-229insGT
ENST00000263816.7:c.2321-230_2321-229insGT	ENSP00000263816.3:n.2321-230_2321-229insGT
ENST00000443831.1:c.1910-230_1910-229insGT	ENSP00000409813.1:n.1910-230_1910-229insGT
NM_004525.2:c.2321-230_2321-229insGT	NP_004516.2:n.2321-230_2321-229insGT
XM_011511183.1:c.2321-230_2321-229insGT	XP_011509485.1:n.2321-230_2321-229insGT
XM_011511184.1:c.32-230_32-229insGT	XP_011509486.1:n.32-230_32-229insGT
XM_011511185.1:c.2321-230_2321-229insGT	XP_011509487.1:n.2321-230_2321-229insGT
NM_004525.3:c.2321-230_2321-229insGT MANE Select	NP_004516.2:n.2321-230_2321-229insGT
XM_011511183.3:c.2321-230_2321-229insGT	XP_011509485.1:n.2321-230_2321-229insGT
XM_011511184.2:c.32-230_32-229insGT	XP_011509486.1:n.32-230_32-229insGT