Canonical Allele Identifier: CA1554172353

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946127G= , CM000667.2:g.70946127G=	GRCh38
NC_000005.9:g.70241954G= , CM000667.1:g.70241954G=	GRCh37
NC_000005.8:g.70277710G=	NCBI36
NG_008691.1:g.26187G= , LRG_676:g.26187G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.785G= MANE Select	ENSP00000370083.4:p.Ser262=
ENST00000351205.8:c.785G=	ENSP00000305857.5:p.Ser262=
ENST00000380707.8:c.785G=	ENSP00000370083.4:p.Ser262=
ENST00000503079.6:c.689G=	ENSP00000428128.1:p.Ser230=
ENST00000506163.5:c.785G=	ENSP00000424926.1:p.Ser262=
ENST00000506239.6:c.785G=	ENSP00000422679.2:p.Ser262=
ENST00000510679.1:n.39G=
ENST00000513228.1:n.352G=
ENST00000514951.5:c.584G=	ENSP00000423298.1:p.Ser195=
ENST00000518504.5:n.302G=
ENST00000625245.2:c.785G=	ENSP00000486539.1:p.Ser262=
NM_000344.3:c.785G= , LRG_676t1:c.785G=	NP_000335.1:p.Ser262=
NM_001297715.1:c.785G=	NP_001284644.1:p.Ser262=
NM_022874.2:c.689G=	NP_075012.1:p.Ser230=
XM_011543596.1:c.785G=	XP_011541898.1:p.Ser262=
XM_011543597.1:c.584G=	XP_011541899.1:p.Ser195=
XM_011543598.1:c.488G=	XP_011541900.1:p.Ser163=
XM_011543598.3:c.488G=	XP_011541900.1:p.Ser163=
XM_017009786.1:c.689G=	XP_016865275.1:p.Ser230=
NM_000344.4:c.785G= MANE Select	NP_000335.1:p.Ser262=