Canonical Allele Identifier: CA2078857727
Gene: MIPEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862246T= , CM000675.2:g.23862246T= GRCh38
NC_000013.10:g.24436385T= , CM000675.1:g.24436385T= GRCh37
NC_000013.9:g.23334385T= NCBI36
NG_052977.1:g.32203A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1053+56A= MANE Select ENSP00000371607.3:n.1053+56A=
ENST00000382172.3:c.1053+56A= ENSP00000371607.3:n.1053+56A=
ENST00000494139.1:n.450+56A=
NM_005932.3:c.1053+56A= NP_005923.2:n.1053+56A=
XM_011535097.1:c.867+56A= XP_011533399.1:n.867+56A=
XM_011535098.1:c.1053+56A= XP_011533400.1:n.1053+56A=
XM_011535097.2:c.867+56A= XP_011533399.1:n.867+56A=
XM_011535098.3:c.1053+56A= XP_011533400.1:n.1053+56A=
NM_005932.4:c.1053+56A= MANE Select NP_005923.3:n.1053+56A=
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