Canonical Allele Identifier: CA1306349813
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247742C= , CM000664.2:g.169247742C= GRCh38
NC_000002.11:g.170104252C= , CM000664.1:g.170104252C= GRCh37
NC_000002.10:g.169812498C= NCBI36
NG_012634.1:g.119871G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2771-227G= MANE Select ENSP00000496870.1:n.2771-227G=
ENST00000263816.7:c.2771-227G= ENSP00000263816.3:n.2771-227G=
ENST00000443831.1:c.2360-227G= ENSP00000409813.1:n.2360-227G=
NM_004525.2:c.2771-227G= NP_004516.2:n.2771-227G=
XM_011511183.1:c.2771-227G= XP_011509485.1:n.2771-227G=
XM_011511184.1:c.482-227G= XP_011509486.1:n.482-227G=
XM_011511185.1:c.2771-227G= XP_011509487.1:n.2771-227G=
NM_004525.3:c.2771-227G= MANE Select NP_004516.2:n.2771-227G=
XM_011511183.3:c.2771-227G= XP_011509485.1:n.2771-227G=
XM_011511184.2:c.482-227G= XP_011509486.1:n.482-227G=
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