Canonical Allele Identifier: CA2078857724
Gene: MIPEP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862245A= , CM000675.2:g.23862245A= GRCh38
NC_000013.10:g.24436384A= , CM000675.1:g.24436384A= GRCh37
NC_000013.9:g.23334384A= NCBI36
NG_052977.1:g.32204T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1053+57T= MANE Select ENSP00000371607.3:n.1053+57T=
ENST00000382172.3:c.1053+57T= ENSP00000371607.3:n.1053+57T=
ENST00000494139.1:n.450+57T=
NM_005932.3:c.1053+57T= NP_005923.2:n.1053+57T=
XM_011535097.1:c.867+57T= XP_011533399.1:n.867+57T=
XM_011535098.1:c.1053+57T= XP_011533400.1:n.1053+57T=
XM_011535097.2:c.867+57T= XP_011533399.1:n.867+57T=
XM_011535098.3:c.1053+57T= XP_011533400.1:n.1053+57T=
NM_005932.4:c.1053+57T= MANE Select NP_005923.3:n.1053+57T=
Search 100 bp 5'
Search 100 bp 3'