Canonical Allele Identifier: CA1306298273
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169128965A= , CM000664.2:g.169128965A= GRCh38
NC_000002.11:g.169985475A= , CM000664.1:g.169985475A= GRCh37
NC_000002.10:g.169693721A= NCBI36
NG_012634.1:g.238648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13800+48T= MANE Select ENSP00000496870.1:n.13800+48T=
ENST00000649153.1:c.4609+48T=
ENST00000650252.1:c.2791+48T= ENSP00000496887.1:n.2791+48T=
ENST00000263816.7:c.13800+48T= ENSP00000263816.3:n.13800+48T=
NM_004525.2:c.13800+48T= NP_004516.2:n.13800+48T=
XM_011511183.1:c.13671+48T= XP_011509485.1:n.13671+48T=
XM_011511184.1:c.11511+48T= XP_011509486.1:n.11511+48T=
NM_004525.3:c.13800+48T= MANE Select NP_004516.2:n.13800+48T=
XM_011511183.3:c.13671+48T= XP_011509485.1:n.13671+48T=
XM_011511184.2:c.11511+48T= XP_011509486.1:n.11511+48T=
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