Canonical Allele Identifier: CA349149041

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.169128986del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128986del , CM000664.2:g.169128986del	GRCh38
NC_000002.11:g.169985496del , CM000664.1:g.169985496del	GRCh37
NC_000002.10:g.169693742del	NCBI36
NG_012634.1:g.238627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+27del MANE Select	ENSP00000496870.1:n.13800+27del
ENST00000649153.1:c.4609+27del
ENST00000650252.1:c.2791+27del	ENSP00000496887.1:n.2791+27del
ENST00000263816.7:c.13800+27del	ENSP00000263816.3:n.13800+27del
NM_004525.2:c.13800+27del	NP_004516.2:n.13800+27del
XM_011511183.1:c.13671+27del	XP_011509485.1:n.13671+27del
XM_011511184.1:c.11511+27del	XP_011509486.1:n.11511+27del
NM_004525.3:c.13800+27del MANE Select	NP_004516.2:n.13800+27del
XM_011511183.3:c.13671+27del	XP_011509485.1:n.13671+27del
XM_011511184.2:c.11511+27del	XP_011509486.1:n.11511+27del