Canonical Allele Identifier: CA1306349817

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247749_169247750delinsAG , CM000664.2:g.169247749_169247750delinsAG	GRCh38
NC_000002.11:g.170104259_170104260delinsAG , CM000664.1:g.170104259_170104260delinsAG	GRCh37
NC_000002.10:g.169812505_169812506delinsAG	NCBI36
NG_012634.1:g.119863_119864delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2771-235_2771-234delinsCT MANE Select	ENSP00000496870.1:n.2771-235_2771-234delinsCT
ENST00000263816.7:c.2771-235_2771-234delinsCT	ENSP00000263816.3:n.2771-235_2771-234delinsCT
ENST00000443831.1:c.2360-235_2360-234delinsCT	ENSP00000409813.1:n.2360-235_2360-234delinsCT
NM_004525.2:c.2771-235_2771-234delinsCT	NP_004516.2:n.2771-235_2771-234delinsCT
XM_011511183.1:c.2771-235_2771-234delinsCT	XP_011509485.1:n.2771-235_2771-234delinsCT
XM_011511184.1:c.482-235_482-234delinsCT	XP_011509486.1:n.482-235_482-234delinsCT
XM_011511185.1:c.2771-235_2771-234delinsCT	XP_011509487.1:n.2771-235_2771-234delinsCT
NM_004525.3:c.2771-235_2771-234delinsCT MANE Select	NP_004516.2:n.2771-235_2771-234delinsCT
XM_011511183.3:c.2771-235_2771-234delinsCT	XP_011509485.1:n.2771-235_2771-234delinsCT
XM_011511184.2:c.482-235_482-234delinsCT	XP_011509486.1:n.482-235_482-234delinsCT