Canonical Allele Identifier: CA1306298272

Gene: LRP2

Linked Data

• dbSNP Id: rs1685189821

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128964T>C , CM000664.2:g.169128964T>C	GRCh38
NC_000002.11:g.169985474T>C , CM000664.1:g.169985474T>C	GRCh37
NC_000002.10:g.169693720T>C	NCBI36
NG_012634.1:g.238649A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+49A>G MANE Select	ENSP00000496870.1:n.13800+49A>G
ENST00000649153.1:c.4609+49A>G
ENST00000650252.1:c.2791+49A>G	ENSP00000496887.1:n.2791+49A>G
ENST00000263816.7:c.13800+49A>G	ENSP00000263816.3:n.13800+49A>G
NM_004525.2:c.13800+49A>G	NP_004516.2:n.13800+49A>G
XM_011511183.1:c.13671+49A>G	XP_011509485.1:n.13671+49A>G
XM_011511184.1:c.11511+49A>G	XP_011509486.1:n.11511+49A>G
NM_004525.3:c.13800+49A>G MANE Select	NP_004516.2:n.13800+49A>G
XM_011511183.3:c.13671+49A>G	XP_011509485.1:n.13671+49A>G
XM_011511184.2:c.11511+49A>G	XP_011509486.1:n.11511+49A>G