Canonical Allele Identifier: CA2078857858
Gene: MIPEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862320_23862324delinsTTTCA , CM000675.2:g.23862320_23862324delinsTTTCA GRCh38
NC_000013.10:g.24436459_24436463delinsTTTCA , CM000675.1:g.24436459_24436463delinsTTTCA GRCh37
NC_000013.9:g.23334459_23334463delinsTTTCA NCBI36
NG_052977.1:g.32125_32129delinsTGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1031_1035delinsTGAAA MANE Select ENSP00000371607.3:p.Met344=
ENST00000382172.3:c.1031_1035delinsTGAAA ENSP00000371607.3:p.Met344=
ENST00000494139.1:n.428_432delinsTGAAA
NM_005932.3:c.1031_1035delinsTGAAA NP_005923.2:p.Met344=
XM_011535097.1:c.845_849delinsTGAAA XP_011533399.1:p.Met282=
XM_011535098.1:c.1031_1035delinsTGAAA XP_011533400.1:p.Met344=
XM_011535097.2:c.845_849delinsTGAAA XP_011533399.1:p.Met282=
XM_011535098.3:c.1031_1035delinsTGAAA XP_011533400.1:p.Met344=
NM_005932.4:c.1031_1035delinsTGAAA MANE Select NP_005923.3:p.Met344=
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