Canonical Allele Identifier: CA2573132196

Gene: NMNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9981124_9981125del , CM000663.2:g.9981124_9981125del	GRCh38
NC_000001.10:g.10041182_10041183del , CM000663.1:g.10041182_10041183del	GRCh37
NC_000001.9:g.9963769_9963770del	NCBI36
NG_032954.1:g.42697_42698del

Transcript Alleles

HGVS	Amino-acid Change
NM_022787.4:c.393_394del MANE Select	NP_073624.2:p.Glu131AspfsTer5
ENST00000377205.6:c.393_394del MANE Select	ENSP00000366410.1:p.Glu131AspfsTer5
NM_001297778.1:c.393_394del	NP_001284707.1:p.Glu131AspfsTer5
NM_001297779.1:c.393_394del	NP_001284708.1:p.Glu131AspfsTer5
NM_001297779.2:c.393_394del	NP_001284708.1:p.Glu131AspfsTer5
NM_022787.3:c.393_394del	NP_073624.2:p.Glu131AspfsTer5
ENST00000377205.5:c.393_394del	ENSP00000366410.1:p.Glu131AspfsTer5
ENST00000403197.5:c.393_394del	ENSP00000385131.1:p.Glu131AspfsTer5
ENST00000462686.1:c.393_394del	ENSP00000435134.1:p.Glu131AspfsTer5
ENST00000496751.1:c.73_74del
XM_011541971.1:c.393_394del	XP_011540273.1:p.Glu131AspfsTer5
XM_011541971.2:c.393_394del	XP_011540273.1:p.Glu131AspfsTer5
XM_017002107.2:c.393_394del	XP_016857596.1:p.Glu131AspfsTer5
XM_017002108.2:c.393_394del	XP_016857597.1:p.Glu131AspfsTer5