Canonical Allele Identifier: CA1306298288

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128992_169128993delinsAG , CM000664.2:g.169128992_169128993delinsAG	GRCh38
NC_000002.11:g.169985502_169985503delinsAG , CM000664.1:g.169985502_169985503delinsAG	GRCh37
NC_000002.10:g.169693748_169693749delinsAG	NCBI36
NG_012634.1:g.238620_238621delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+20_13800+21delinsCT MANE Select	ENSP00000496870.1:n.13800+20_13800+21delinsCT
ENST00000649153.1:c.4609+20_4609+21delinsCT
ENST00000650252.1:c.2791+20_2791+21delinsCT	ENSP00000496887.1:n.2791+20_2791+21delinsCT
ENST00000263816.7:c.13800+20_13800+21delinsCT	ENSP00000263816.3:n.13800+20_13800+21delinsCT
NM_004525.2:c.13800+20_13800+21delinsCT	NP_004516.2:n.13800+20_13800+21delinsCT
XM_011511183.1:c.13671+20_13671+21delinsCT	XP_011509485.1:n.13671+20_13671+21delinsCT
XM_011511184.1:c.11511+20_11511+21delinsCT	XP_011509486.1:n.11511+20_11511+21delinsCT
NM_004525.3:c.13800+20_13800+21delinsCT MANE Select	NP_004516.2:n.13800+20_13800+21delinsCT
XM_011511183.3:c.13671+20_13671+21delinsCT	XP_011509485.1:n.13671+20_13671+21delinsCT
XM_011511184.2:c.11511+20_11511+21delinsCT	XP_011509486.1:n.11511+20_11511+21delinsCT