Canonical Allele Identifier: CA1306353633

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169258866_169258867delinsGT , CM000664.2:g.169258866_169258867delinsGT	GRCh38
NC_000002.11:g.170115376_170115377delinsGT , CM000664.1:g.170115376_170115377delinsGT	GRCh37
NC_000002.10:g.169823622_169823623delinsGT	NCBI36
NG_012634.1:g.108746_108747delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+158_2513+159delinsAC MANE Select	ENSP00000496870.1:n.2513+158_2513+159delinsAC
ENST00000263816.7:c.2513+158_2513+159delinsAC	ENSP00000263816.3:n.2513+158_2513+159delinsAC
ENST00000443831.1:c.2102+158_2102+159delinsAC	ENSP00000409813.1:n.2102+158_2102+159delinsAC
NM_004525.2:c.2513+158_2513+159delinsAC	NP_004516.2:n.2513+158_2513+159delinsAC
XM_011511183.1:c.2513+158_2513+159delinsAC	XP_011509485.1:n.2513+158_2513+159delinsAC
XM_011511184.1:c.224+158_224+159delinsAC	XP_011509486.1:n.224+158_224+159delinsAC
XM_011511185.1:c.2513+158_2513+159delinsAC	XP_011509487.1:n.2513+158_2513+159delinsAC
NM_004525.3:c.2513+158_2513+159delinsAC MANE Select	NP_004516.2:n.2513+158_2513+159delinsAC
XM_011511183.3:c.2513+158_2513+159delinsAC	XP_011509485.1:n.2513+158_2513+159delinsAC
XM_011511184.2:c.224+158_224+159delinsAC	XP_011509486.1:n.224+158_224+159delinsAC