Canonical Allele Identifier: CA1554171487
Gene: SMN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70942364G= , CM000667.2:g.70942364G= GRCh38
NC_000005.9:g.70238191G= , CM000667.1:g.70238191G= GRCh37
NC_000005.8:g.70273947G= NCBI36
NG_008691.1:g.22424G= , LRG_676:g.22424G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.280G= MANE Select ENSP00000370083.4:p.Val94=
ENST00000351205.8:c.280G= ENSP00000305857.5:p.Val94=
ENST00000380707.8:c.280G= ENSP00000370083.4:p.Val94=
ENST00000503079.6:c.280G= ENSP00000428128.1:p.Val94=
ENST00000506163.5:c.280G= ENSP00000424926.1:p.Val94=
ENST00000506239.6:c.280G= ENSP00000422679.2:p.Val94=
ENST00000514951.5:c.274-354G= ENSP00000423298.1:n.274-354G=
ENST00000625245.2:c.280G= ENSP00000486539.1:p.Val94=
NM_000344.3:c.280G= , LRG_676t1:c.280G= NP_000335.1:p.Val94=
NM_001297715.1:c.280G= NP_001284644.1:p.Val94=
NM_022874.2:c.280G= NP_075012.1:p.Val94=
XM_011543596.1:c.280G= XP_011541898.1:p.Val94=
XM_011543597.1:c.274-354G= XP_011541899.1:n.274-354G=
XM_011543598.1:c.274-354G= XP_011541900.1:n.274-354G=
XM_011543598.3:c.274-354G= XP_011541900.1:n.274-354G=
XM_017009786.1:c.280G= XP_016865275.1:p.Val94=
NM_000344.4:c.280G= MANE Select NP_000335.1:p.Val94=