Canonical Allele Identifier: CA387526003
Gene: MIPEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862306T>A , CM000675.2:g.23862306T>A GRCh38
NC_000013.10:g.24436445T>A , CM000675.1:g.24436445T>A GRCh37
NC_000013.9:g.23334445T>A NCBI36
NG_052977.1:g.32143A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1049A>T MANE Select ENSP00000371607.3:p.Asn350Ile
ENST00000382172.3:c.1049A>T ENSP00000371607.3:p.Asn350Ile
ENST00000494139.1:n.446A>T
NM_005932.3:c.1049A>T NP_005923.2:p.Asn350Ile
XM_011535097.1:c.863A>T XP_011533399.1:p.Asn288Ile
XM_011535098.1:c.1049A>T XP_011533400.1:p.Asn350Ile
XM_011535097.2:c.863A>T XP_011533399.1:p.Asn288Ile
XM_011535098.3:c.1049A>T XP_011533400.1:p.Asn350Ile
NM_005932.4:c.1049A>T MANE Select NP_005923.3:p.Asn350Ile