Canonical Allele Identifier: CA360097315
Gene: SMN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70946168T>G , CM000667.2:g.70946168T>G GRCh38
NC_000005.9:g.70241995T>G , CM000667.1:g.70241995T>G GRCh37
NC_000005.8:g.70277751T>G NCBI36
NG_008691.1:g.26228T>G , LRG_676:g.26228T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.826T>G MANE Select ENSP00000370083.4:p.Tyr276Asp
ENST00000351205.8:c.826T>G ENSP00000305857.5:p.Tyr276Asp
ENST00000380707.8:c.826T>G ENSP00000370083.4:p.Tyr276Asp
ENST00000503079.6:c.730T>G ENSP00000428128.1:p.Tyr244Asp
ENST00000506163.5:c.826T>G ENSP00000424926.1:p.Tyr276Asp
ENST00000506239.6:c.826T>G ENSP00000422679.2:p.Tyr276Asp
ENST00000510679.1:n.80T>G
ENST00000513228.1:n.393T>G
ENST00000514951.5:c.625T>G ENSP00000423298.1:p.Tyr209Asp
ENST00000518504.5:n.343T>G
ENST00000625245.2:c.826T>G ENSP00000486539.1:p.Tyr276Asp
NM_000344.3:c.826T>G , LRG_676t1:c.826T>G NP_000335.1:p.Tyr276Asp
NM_001297715.1:c.826T>G NP_001284644.1:p.Tyr276Asp
NM_022874.2:c.730T>G NP_075012.1:p.Tyr244Asp
XM_011543596.1:c.826T>G XP_011541898.1:p.Tyr276Asp
XM_011543597.1:c.625T>G XP_011541899.1:p.Tyr209Asp
XM_011543598.1:c.529T>G XP_011541900.1:p.Tyr177Asp
XM_011543598.3:c.529T>G XP_011541900.1:p.Tyr177Asp
XM_017009786.1:c.730T>G XP_016865275.1:p.Tyr244Asp
NM_000344.4:c.826T>G MANE Select NP_000335.1:p.Tyr276Asp