Canonical Allele Identifier: CA1554174123

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70951951A= , CM000667.2:g.70951951A=	GRCh38
NC_000005.9:g.70247778A= , CM000667.1:g.70247778A=	GRCh37
NC_000005.8:g.70283534A=	NCBI36
NG_008691.1:g.32011A= , LRG_676:g.32011A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380707.9:c.845A= MANE Select	ENSP00000370083.4:p.Gln282=
ENST00000351205.8:c.845A=	ENSP00000305857.5:p.Gln282=
ENST00000380707.8:c.845A=	ENSP00000370083.4:p.Gln282=
ENST00000503079.6:c.749A=	ENSP00000428128.1:p.Gln250=
ENST00000506163.5:c.835-488A=	ENSP00000424926.1:n.835-488A=
ENST00000506239.6:c.*59-488A=	ENSP00000422679.2:n.*59-488A=
ENST00000510679.1:n.99A=
ENST00000514951.5:c.644A=	ENSP00000423298.1:p.Gln215=
NM_000344.3:c.845A= , LRG_676t1:c.845A=	NP_000335.1:p.Gln282=
NM_001297715.1:c.835-488A=	NP_001284644.1:n.835-488A=
NM_022874.2:c.749A=	NP_075012.1:p.Gln250=
XM_011543597.1:c.644A=	XP_011541899.1:p.Gln215=
XM_011543598.1:c.548A=	XP_011541900.1:p.Gln183=
XM_011543598.3:c.548A=	XP_011541900.1:p.Gln183=
XM_017009786.1:c.739-488A=	XP_016865275.1:n.739-488A=
NM_000344.4:c.845A= MANE Select	NP_000335.1:p.Gln282=