Canonical Allele Identifier: CA1554044331

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076532A= , CM000667.2:g.70076532A=	GRCh38
NC_000005.9:g.69372359A= , CM000667.1:g.69372359A=	GRCh37
NC_000005.8:g.69408115A=	NCBI36
NG_008728.1:g.32010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.846A= MANE Select	ENSP00000370119.4:p.Gln282=
ENST00000380741.8:c.846A=	ENSP00000370117.5:p.Gln282=
ENST00000380742.8:c.750A=	ENSP00000370118.4:p.Gln250=
ENST00000380743.8:c.846A=	ENSP00000370119.4:p.Gln282=
ENST00000505346.5:n.312A=
ENST00000506734.5:c.*59-487A=	ENSP00000424799.1:n.*59-487A=
ENST00000507458.2:c.100A=
ENST00000511812.5:c.645A=	ENSP00000424282.1:p.Gln215=
ENST00000514914.1:n.387A=
ENST00000614240.4:c.750A=	ENSP00000479279.1:p.Gln250=
ENST00000626847.2:c.835-487A=	ENSP00000486152.1:n.835-487A=
NM_017411.3:c.846A=	NP_059107.1:p.Gln282=
NM_022875.2:c.835-487A=	NP_075013.1:n.835-487A=
NM_022876.2:c.750A=	NP_075014.1:p.Gln250=
NM_022877.2:c.739-487A=	NP_075015.1:n.739-487A=
XM_011543600.1:c.645A=	XP_011541902.1:p.Gln215=
XM_011543601.1:c.634-487A=	XP_011541903.1:n.634-487A=
XM_011543602.1:c.549A=	XP_011541904.1:p.Gln183=
XM_011543603.1:c.538-487A=	XP_011541905.1:n.538-487A=
XR_948432.1:n.1054+88528A=
XM_011543600.2:c.645A=	XP_011541902.1:p.Gln215=
XM_011543602.3:c.549A=	XP_011541904.1:p.Gln183=
XM_011543603.3:c.538-487A=	XP_011541905.1:n.538-487A=
NM_017411.4:c.846A= MANE Select	NP_059107.1:p.Gln282=
NM_022875.3:c.835-487A=	NP_075013.1:n.835-487A=