Canonical Allele Identifier: CA2078889198
Community Standard Title: NM_005932.4(MIPEP):c.212T= (p.Leu71=)
Gene: MIPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23886484A= , CM000675.2:g.23886484A= GRCh38
NC_000013.10:g.24460623A= , CM000675.1:g.24460623A= GRCh37
NC_000013.9:g.23358623A= NCBI36
NG_052977.1:g.7965T=

Transcript Alleles

HGVS Amino-acid Change
NM_005932.4:c.212T= MANE Select NP_005923.3:p.Leu71=
ENST00000382172.4:c.212T= MANE Select ENSP00000371607.3:p.Leu71=
NM_005932.3:c.212T= NP_005923.2:p.Leu71=
ENST00000382172.3:c.212T= ENSP00000371607.3:p.Leu71=
ENST00000469167.1:n.744T=
XM_011535097.1:c.26T= XP_011533399.1:p.Leu9=
XM_011535097.2:c.26T= XP_011533399.1:p.Leu9=
XM_011535098.1:c.212T= XP_011533400.1:p.Leu71=
XM_011535098.3:c.212T= XP_011533400.1:p.Leu71=