Canonical Allele Identifier: CA1306298281
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169128985T= , CM000664.2:g.169128985T= GRCh38
NC_000002.11:g.169985495T= , CM000664.1:g.169985495T= GRCh37
NC_000002.10:g.169693741T= NCBI36
NG_012634.1:g.238628A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13800+28A= MANE Select ENSP00000496870.1:n.13800+28A=
ENST00000649153.1:c.4609+28A=
ENST00000650252.1:c.2791+28A= ENSP00000496887.1:n.2791+28A=
ENST00000263816.7:c.13800+28A= ENSP00000263816.3:n.13800+28A=
NM_004525.2:c.13800+28A= NP_004516.2:n.13800+28A=
XM_011511183.1:c.13671+28A= XP_011509485.1:n.13671+28A=
XM_011511184.1:c.11511+28A= XP_011509486.1:n.11511+28A=
NM_004525.3:c.13800+28A= MANE Select NP_004516.2:n.13800+28A=
XM_011511183.3:c.13671+28A= XP_011509485.1:n.13671+28A=
XM_011511184.2:c.11511+28A= XP_011509486.1:n.11511+28A=
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