Canonical Allele Identifier: CA1554174125
Gene: SMN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70951956C= , CM000667.2:g.70951956C= GRCh38
NC_000005.9:g.70247783C= , CM000667.1:g.70247783C= GRCh37
NC_000005.8:g.70283539C= NCBI36
NG_008691.1:g.32016C= , LRG_676:g.32016C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380707.9:c.850C= MANE Select ENSP00000370083.4:p.Gln284=
ENST00000351205.8:c.850C= ENSP00000305857.5:p.Gln284=
ENST00000380707.8:c.850C= ENSP00000370083.4:p.Gln284=
ENST00000503079.6:c.754C= ENSP00000428128.1:p.Gln252=
ENST00000506163.5:c.835-483C= ENSP00000424926.1:n.835-483C=
ENST00000506239.6:c.*59-483C= ENSP00000422679.2:n.*59-483C=
ENST00000510679.1:n.104C=
ENST00000514951.5:c.649C= ENSP00000423298.1:p.Gln217=
NM_000344.3:c.850C= , LRG_676t1:c.850C= NP_000335.1:p.Gln284=
NM_001297715.1:c.835-483C= NP_001284644.1:n.835-483C=
NM_022874.2:c.754C= NP_075012.1:p.Gln252=
XM_011543597.1:c.649C= XP_011541899.1:p.Gln217=
XM_011543598.1:c.553C= XP_011541900.1:p.Gln185=
XM_011543598.3:c.553C= XP_011541900.1:p.Gln185=
XM_017009786.1:c.739-483C= XP_016865275.1:n.739-483C=
NM_000344.4:c.850C= MANE Select NP_000335.1:p.Gln284=