Canonical Allele Identifier: CA2573157523
Community Standard Title: NM_003906.5(MCM3AP):c.3421del (p.Glu1141LysfsTer17)
Gene: MCM3AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46261327del , CM000683.2:g.46261327del GRCh38
NC_000021.8:g.47681241del , CM000683.1:g.47681241del GRCh37
NC_000021.7:g.46505669del NCBI36
NG_033881.1:g.28997del

Transcript Alleles

HGVS Amino-acid Change
NM_003906.5:c.3421del MANE Select NP_003897.2:p.Glu1141LysfsTer17
ENST00000291688.6:c.3421del MANE Select ENSP00000291688.1:p.Glu1141LysfsTer17
NM_003906.4:c.3421del NP_003897.2:p.Glu1141LysfsTer17
ENST00000291688.5:c.3421del ENSP00000291688.1:p.Glu1141LysfsTer17
ENST00000397708.1:c.3421del ENSP00000380820.1:p.Glu1141LysfsTer17
ENST00000486937.5:n.1713del
ENST00000496607.5:n.1418del
XM_005261203.3:c.3421del XP_005261260.1:p.Glu1141LysfsTer17
XM_005261203.4:c.3421del XP_005261260.1:p.Glu1141LysfsTer17
XM_005261204.3:c.3421del XP_005261261.1:p.Glu1141LysfsTer17
XM_005261204.5:c.3421del XP_005261261.1:p.Glu1141LysfsTer17
XM_005261205.2:c.3421del XP_005261262.1:p.Glu1141LysfsTer17
XM_005261205.4:c.3421del XP_005261262.1:p.Glu1141LysfsTer17
XM_005261206.3:c.3421del XP_005261263.1:p.Glu1141LysfsTer17
XM_006724064.2:c.3421del XP_006724127.1:p.Glu1141LysfsTer17
XR_937577.1:n.4010del