Canonical Allele Identifier: CA1554172350

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946109A= , CM000667.2:g.70946109A=	GRCh38
NC_000005.9:g.70241936A= , CM000667.1:g.70241936A=	GRCh37
NC_000005.8:g.70277692A=	NCBI36
NG_008691.1:g.26169A= , LRG_676:g.26169A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.767A= MANE Select	ENSP00000370083.4:p.Asp256=
ENST00000351205.8:c.767A=	ENSP00000305857.5:p.Asp256=
ENST00000380707.8:c.767A=	ENSP00000370083.4:p.Asp256=
ENST00000503079.6:c.671A=	ENSP00000428128.1:p.Asp224=
ENST00000506163.5:c.767A=	ENSP00000424926.1:p.Asp256=
ENST00000506239.6:c.767A=	ENSP00000422679.2:p.Asp256=
ENST00000510679.1:n.21A=
ENST00000513228.1:n.334A=
ENST00000514951.5:c.566A=	ENSP00000423298.1:p.Asp189=
ENST00000518504.5:n.284A=
ENST00000625245.2:c.767A=	ENSP00000486539.1:p.Asp256=
NM_000344.3:c.767A= , LRG_676t1:c.767A=	NP_000335.1:p.Asp256=
NM_001297715.1:c.767A=	NP_001284644.1:p.Asp256=
NM_022874.2:c.671A=	NP_075012.1:p.Asp224=
XM_011543596.1:c.767A=	XP_011541898.1:p.Asp256=
XM_011543597.1:c.566A=	XP_011541899.1:p.Asp189=
XM_011543598.1:c.470A=	XP_011541900.1:p.Asp157=
XM_011543598.3:c.470A=	XP_011541900.1:p.Asp157=
XM_017009786.1:c.671A=	XP_016865275.1:p.Asp224=
NM_000344.4:c.767A= MANE Select	NP_000335.1:p.Asp256=