Canonical Allele Identifier: CA1306298279

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128984_169128985delinsCT , CM000664.2:g.169128984_169128985delinsCT	GRCh38
NC_000002.11:g.169985494_169985495delinsCT , CM000664.1:g.169985494_169985495delinsCT	GRCh37
NC_000002.10:g.169693740_169693741delinsCT	NCBI36
NG_012634.1:g.238628_238629delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+28_13800+29delinsAG MANE Select	ENSP00000496870.1:n.13800+28_13800+29delinsAG
ENST00000649153.1:c.4609+28_4609+29delinsAG
ENST00000650252.1:c.2791+28_2791+29delinsAG	ENSP00000496887.1:n.2791+28_2791+29delinsAG
ENST00000263816.7:c.13800+28_13800+29delinsAG	ENSP00000263816.3:n.13800+28_13800+29delinsAG
NM_004525.2:c.13800+28_13800+29delinsAG	NP_004516.2:n.13800+28_13800+29delinsAG
XM_011511183.1:c.13671+28_13671+29delinsAG	XP_011509485.1:n.13671+28_13671+29delinsAG
XM_011511184.1:c.11511+28_11511+29delinsAG	XP_011509486.1:n.11511+28_11511+29delinsAG
NM_004525.3:c.13800+28_13800+29delinsAG MANE Select	NP_004516.2:n.13800+28_13800+29delinsAG
XM_011511183.3:c.13671+28_13671+29delinsAG	XP_011509485.1:n.13671+28_13671+29delinsAG
XM_011511184.2:c.11511+28_11511+29delinsAG	XP_011509486.1:n.11511+28_11511+29delinsAG