Canonical Allele Identifier: CA1306298271
Gene: LRP2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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