Canonical Allele Identifier: CA2661823049

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259344-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259344_169259345insA , CM000664.2:g.169259344_169259345insA	GRCh38
NC_000002.11:g.170115854_170115855insA , CM000664.1:g.170115854_170115855insA	GRCh37
NC_000002.10:g.169824100_169824101insA	NCBI36
NG_012634.1:g.108268_108269insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-128_2321-127insT MANE Select	ENSP00000496870.1:n.2321-128_2321-127insT
ENST00000263816.7:c.2321-128_2321-127insT	ENSP00000263816.3:n.2321-128_2321-127insT
ENST00000443831.1:c.1910-128_1910-127insT	ENSP00000409813.1:n.1910-128_1910-127insT
NM_004525.2:c.2321-128_2321-127insT	NP_004516.2:n.2321-128_2321-127insT
XM_011511183.1:c.2321-128_2321-127insT	XP_011509485.1:n.2321-128_2321-127insT
XM_011511184.1:c.32-128_32-127insT	XP_011509486.1:n.32-128_32-127insT
XM_011511185.1:c.2321-128_2321-127insT	XP_011509487.1:n.2321-128_2321-127insT
NM_004525.3:c.2321-128_2321-127insT MANE Select	NP_004516.2:n.2321-128_2321-127insT
XM_011511183.3:c.2321-128_2321-127insT	XP_011509485.1:n.2321-128_2321-127insT
XM_011511184.2:c.32-128_32-127insT	XP_011509486.1:n.32-128_32-127insT