Canonical Allele Identifier: CA1306353653
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169258913T= , CM000664.2:g.169258913T= GRCh38
NC_000002.11:g.170115423T= , CM000664.1:g.170115423T= GRCh37
NC_000002.10:g.169823669T= NCBI36
NG_012634.1:g.108700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2513+112A= MANE Select ENSP00000496870.1:n.2513+112A=
ENST00000263816.7:c.2513+112A= ENSP00000263816.3:n.2513+112A=
ENST00000443831.1:c.2102+112A= ENSP00000409813.1:n.2102+112A=
NM_004525.2:c.2513+112A= NP_004516.2:n.2513+112A=
XM_011511183.1:c.2513+112A= XP_011509485.1:n.2513+112A=
XM_011511184.1:c.224+112A= XP_011509486.1:n.224+112A=
XM_011511185.1:c.2513+112A= XP_011509487.1:n.2513+112A=
NM_004525.3:c.2513+112A= MANE Select NP_004516.2:n.2513+112A=
XM_011511183.3:c.2513+112A= XP_011509485.1:n.2513+112A=
XM_011511184.2:c.224+112A= XP_011509486.1:n.224+112A=
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