Canonical Allele Identifier: CA2575370329
Gene: MIPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862299del , CM000675.2:g.23862299del GRCh38
NC_000013.10:g.24436438del , CM000675.1:g.24436438del GRCh37
NC_000013.9:g.23334438del NCBI36
NG_052977.1:g.32151del

Transcript Alleles

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