Canonical Allele Identifier: CA360092164
Gene: SMN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70938897T>A , CM000667.2:g.70938897T>A GRCh38
NC_000005.9:g.70234724T>A , CM000667.1:g.70234724T>A GRCh37
NC_000005.8:g.70270480T>A NCBI36
NG_008691.1:g.18957T>A , LRG_676:g.18957T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.140T>A MANE Select ENSP00000370083.4:p.Val47Glu
ENST00000351205.8:c.140T>A ENSP00000305857.5:p.Val47Glu
ENST00000380707.8:c.140T>A ENSP00000370083.4:p.Val47Glu
ENST00000503079.6:c.140T>A ENSP00000428128.1:p.Val47Glu
ENST00000506163.5:c.140T>A ENSP00000424926.1:p.Val47Glu
ENST00000506239.6:c.140T>A ENSP00000422679.2:p.Val47Glu
ENST00000514951.5:c.140T>A ENSP00000423298.1:p.Val47Glu
ENST00000625245.2:c.140T>A ENSP00000486539.1:p.Val47Glu
NM_000344.3:c.140T>A , LRG_676t1:c.140T>A NP_000335.1:p.Val47Glu
NM_001297715.1:c.140T>A NP_001284644.1:p.Val47Glu
NM_022874.2:c.140T>A NP_075012.1:p.Val47Glu
XM_011543596.1:c.140T>A XP_011541898.1:p.Val47Glu
XM_011543597.1:c.140T>A XP_011541899.1:p.Val47Glu
XM_011543598.1:c.140T>A XP_011541900.1:p.Val47Glu
XM_011543598.3:c.140T>A XP_011541900.1:p.Val47Glu
XM_017009786.1:c.140T>A XP_016865275.1:p.Val47Glu
NM_000344.4:c.140T>A MANE Select NP_000335.1:p.Val47Glu