Canonical Allele Identifier: CA2661813271

Gene: LRP2

Linked Data

• gnomAD v4: 2-169128968-TTCTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128969_169128973del , CM000664.2:g.169128969_169128973del	GRCh38
NC_000002.11:g.169985479_169985483del , CM000664.1:g.169985479_169985483del	GRCh37
NC_000002.10:g.169693725_169693729del	NCBI36
NG_012634.1:g.238640_238644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+40_13800+44del MANE Select	ENSP00000496870.1:n.13800+40_13800+44del
ENST00000649153.1:c.4609+40_4609+44del
ENST00000650252.1:c.2791+40_2791+44del	ENSP00000496887.1:n.2791+40_2791+44del
ENST00000263816.7:c.13800+40_13800+44del	ENSP00000263816.3:n.13800+40_13800+44del
NM_004525.2:c.13800+40_13800+44del	NP_004516.2:n.13800+40_13800+44del
XM_011511183.1:c.13671+40_13671+44del	XP_011509485.1:n.13671+40_13671+44del
XM_011511184.1:c.11511+40_11511+44del	XP_011509486.1:n.11511+40_11511+44del
NM_004525.3:c.13800+40_13800+44del MANE Select	NP_004516.2:n.13800+40_13800+44del
XM_011511183.3:c.13671+40_13671+44del	XP_011509485.1:n.13671+40_13671+44del
XM_011511184.2:c.11511+40_11511+44del	XP_011509486.1:n.11511+40_11511+44del