Canonical Allele Identifier: CA338686033
Community Standard Title: NM_022787.4(NMNAT1):c.376A>T (p.Lys126Ter)
Gene: NMNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9981107A>T , CM000663.2:g.9981107A>T GRCh38
NC_000001.10:g.10041165A>T , CM000663.1:g.10041165A>T GRCh37
NC_000001.9:g.9963752A>T NCBI36
NG_032954.1:g.42680A>T

Transcript Alleles

HGVS Amino-acid Change
NM_022787.4:c.376A>T MANE Select NP_073624.2:p.Lys126Ter
ENST00000377205.6:c.376A>T MANE Select ENSP00000366410.1:p.Lys126Ter
NM_001297778.1:c.376A>T NP_001284707.1:p.Lys126Ter
NM_001297779.1:c.376A>T NP_001284708.1:p.Lys126Ter
NM_001297779.2:c.376A>T NP_001284708.1:p.Lys126Ter
NM_022787.3:c.376A>T NP_073624.2:p.Lys126Ter
ENST00000377205.5:c.376A>T ENSP00000366410.1:p.Lys126Ter
ENST00000403197.5:c.376A>T ENSP00000385131.1:p.Lys126Ter
ENST00000462686.1:c.376A>T ENSP00000435134.1:p.Lys126Ter
ENST00000496751.1:c.56A>T
XM_011541971.1:c.376A>T XP_011540273.1:p.Lys126Ter
XM_011541971.2:c.376A>T XP_011540273.1:p.Lys126Ter
XM_017002107.2:c.376A>T XP_016857596.1:p.Lys126Ter
XM_017002108.2:c.376A>T XP_016857597.1:p.Lys126Ter