Canonical Allele Identifier: CA1554174121

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70951950C= , CM000667.2:g.70951950C=	GRCh38
NC_000005.9:g.70247777C= , CM000667.1:g.70247777C=	GRCh37
NC_000005.8:g.70283533C=	NCBI36
NG_008691.1:g.32010C= , LRG_676:g.32010C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380707.9:c.844C= MANE Select	ENSP00000370083.4:p.Gln282=
ENST00000351205.8:c.844C=	ENSP00000305857.5:p.Gln282=
ENST00000380707.8:c.844C=	ENSP00000370083.4:p.Gln282=
ENST00000503079.6:c.748C=	ENSP00000428128.1:p.Gln250=
ENST00000506163.5:c.835-489C=	ENSP00000424926.1:n.835-489C=
ENST00000506239.6:c.*59-489C=	ENSP00000422679.2:n.*59-489C=
ENST00000510679.1:n.98C=
ENST00000514951.5:c.643C=	ENSP00000423298.1:p.Gln215=
NM_000344.3:c.844C= , LRG_676t1:c.844C=	NP_000335.1:p.Gln282=
NM_001297715.1:c.835-489C=	NP_001284644.1:n.835-489C=
NM_022874.2:c.748C=	NP_075012.1:p.Gln250=
XM_011543597.1:c.643C=	XP_011541899.1:p.Gln215=
XM_011543598.1:c.547C=	XP_011541900.1:p.Gln183=
XM_011543598.3:c.547C=	XP_011541900.1:p.Gln183=
XM_017009786.1:c.739-489C=	XP_016865275.1:n.739-489C=
NM_000344.4:c.844C= MANE Select	NP_000335.1:p.Gln282=