Canonical Allele Identifier: CA1554174112
Gene: SMN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70951939A= , CM000667.2:g.70951939A= GRCh38
NC_000005.9:g.70247766A= , CM000667.1:g.70247766A= GRCh37
NC_000005.8:g.70283522A= NCBI36
NG_008691.1:g.31999A= , LRG_676:g.31999A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380707.9:c.835-2A= MANE Select ENSP00000370083.4:n.835-2A=
ENST00000351205.8:c.835-2A= ENSP00000305857.5:n.835-2A=
ENST00000380707.8:c.835-2A= ENSP00000370083.4:n.835-2A=
ENST00000503079.6:c.739-2A= ENSP00000428128.1:n.739-2A=
ENST00000506163.5:c.835-500A= ENSP00000424926.1:n.835-500A=
ENST00000506239.6:c.*59-500A= ENSP00000422679.2:n.*59-500A=
ENST00000510679.1:n.89-2A=
ENST00000514951.5:c.634-2A= ENSP00000423298.1:n.634-2A=
NM_000344.3:c.835-2A= , LRG_676t1:c.835-2A= NP_000335.1:n.835-2A=
NM_001297715.1:c.835-500A= NP_001284644.1:n.835-500A=
NM_022874.2:c.739-2A= NP_075012.1:n.739-2A=
XM_011543597.1:c.634-2A= XP_011541899.1:n.634-2A=
XM_011543598.1:c.538-2A= XP_011541900.1:n.538-2A=
XM_011543598.3:c.538-2A= XP_011541900.1:n.538-2A=
XM_017009786.1:c.739-500A= XP_016865275.1:n.739-500A=
NM_000344.4:c.835-2A= MANE Select NP_000335.1:n.835-2A=