Canonical Allele Identifier: CA360096936
Gene: SMN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70946123G>C , CM000667.2:g.70946123G>C GRCh38
NC_000005.9:g.70241950G>C , CM000667.1:g.70241950G>C GRCh37
NC_000005.8:g.70277706G>C NCBI36
NG_008691.1:g.26183G>C , LRG_676:g.26183G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380707.9:c.781G>C MANE Select ENSP00000370083.4:p.Gly261Arg
ENST00000351205.8:c.781G>C ENSP00000305857.5:p.Gly261Arg
ENST00000380707.8:c.781G>C ENSP00000370083.4:p.Gly261Arg
ENST00000503079.6:c.685G>C ENSP00000428128.1:p.Gly229Arg
ENST00000506163.5:c.781G>C ENSP00000424926.1:p.Gly261Arg
ENST00000506239.6:c.781G>C ENSP00000422679.2:p.Gly261Arg
ENST00000510679.1:n.35G>C
ENST00000513228.1:n.348G>C
ENST00000514951.5:c.580G>C ENSP00000423298.1:p.Gly194Arg
ENST00000518504.5:n.298G>C
ENST00000625245.2:c.781G>C ENSP00000486539.1:p.Gly261Arg
NM_000344.3:c.781G>C , LRG_676t1:c.781G>C NP_000335.1:p.Gly261Arg
NM_001297715.1:c.781G>C NP_001284644.1:p.Gly261Arg
NM_022874.2:c.685G>C NP_075012.1:p.Gly229Arg
XM_011543596.1:c.781G>C XP_011541898.1:p.Gly261Arg
XM_011543597.1:c.580G>C XP_011541899.1:p.Gly194Arg
XM_011543598.1:c.484G>C XP_011541900.1:p.Gly162Arg
XM_011543598.3:c.484G>C XP_011541900.1:p.Gly162Arg
XM_017009786.1:c.685G>C XP_016865275.1:p.Gly229Arg
NM_000344.4:c.781G>C MANE Select NP_000335.1:p.Gly261Arg