Canonical Allele Identifier: CA1554172332
Gene: SMN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70945940G= , CM000667.2:g.70945940G= GRCh38
NC_000005.9:g.70241767G= , CM000667.1:g.70241767G= GRCh37
NC_000005.8:g.70277523G= NCBI36
NG_008691.1:g.26000G= , LRG_676:g.26000G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.724-126G= MANE Select ENSP00000370083.4:n.724-126G=
ENST00000351205.8:c.724-126G= ENSP00000305857.5:n.724-126G=
ENST00000380707.8:c.724-126G= ENSP00000370083.4:n.724-126G=
ENST00000503079.6:c.628-126G= ENSP00000428128.1:n.628-126G=
ENST00000506163.5:c.724-126G= ENSP00000424926.1:n.724-126G=
ENST00000506239.6:c.724-126G= ENSP00000422679.2:n.724-126G=
ENST00000507905.6:c.418-126G= ENSP00000430657.1:n.418-126G=
ENST00000513228.1:n.291-126G=
ENST00000514951.5:c.523-126G= ENSP00000423298.1:n.523-126G=
ENST00000518504.5:n.241-126G=
ENST00000625245.2:c.724-126G= ENSP00000486539.1:n.724-126G=
NM_000344.3:c.724-126G= , LRG_676t1:c.724-126G= NP_000335.1:n.724-126G=
NM_001297715.1:c.724-126G= NP_001284644.1:n.724-126G=
NM_022874.2:c.628-126G= NP_075012.1:n.628-126G=
XM_011543596.1:c.724-126G= XP_011541898.1:n.724-126G=
XM_011543597.1:c.523-126G= XP_011541899.1:n.523-126G=
XM_011543598.1:c.427-126G= XP_011541900.1:n.427-126G=
XM_011543598.3:c.427-126G= XP_011541900.1:n.427-126G=
XM_017009786.1:c.628-126G= XP_016865275.1:n.628-126G=
NM_000344.4:c.724-126G= MANE Select NP_000335.1:n.724-126G=