Canonical Allele Identifier: CA360096491
Gene: SMN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70946065G>T , CM000667.2:g.70946065G>T GRCh38
NC_000005.9:g.70241892G>T , CM000667.1:g.70241892G>T GRCh37
NC_000005.8:g.70277648G>T NCBI36
NG_008691.1:g.26125G>T , LRG_676:g.26125G>T

Transcript Alleles

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