Canonical Allele Identifier: CA2622340353
Gene: MIPEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862316del , CM000675.2:g.23862316del GRCh38
NC_000013.10:g.24436455del , CM000675.1:g.24436455del GRCh37
NC_000013.9:g.23334455del NCBI36
NG_052977.1:g.32134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1040del MANE Select ENSP00000371607.3:p.Asn347IlefsTer7
ENST00000382172.3:c.1040del ENSP00000371607.3:p.Asn347IlefsTer7
ENST00000494139.1:n.437del
NM_005932.3:c.1040del NP_005923.2:p.Asn347IlefsTer7
XM_011535097.1:c.854del XP_011533399.1:p.Asn285IlefsTer7
XM_011535098.1:c.1040del XP_011533400.1:p.Asn347IlefsTer7
XM_011535097.2:c.854del XP_011533399.1:p.Asn285IlefsTer7
XM_011535098.3:c.1040del XP_011533400.1:p.Asn347IlefsTer7
NM_005932.4:c.1040del MANE Select NP_005923.3:p.Asn347IlefsTer7