Canonical Allele Identifier: CA1554044294

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076443A= , CM000667.2:g.70076443A=	GRCh38
NC_000005.9:g.69372270A= , CM000667.1:g.69372270A=	GRCh37
NC_000005.8:g.69408026A=	NCBI36
NG_008728.1:g.31921A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.835-78A= MANE Select	ENSP00000370119.4:n.835-78A=
ENST00000380741.8:c.835-78A=	ENSP00000370117.5:n.835-78A=
ENST00000380742.8:c.739-78A=	ENSP00000370118.4:n.739-78A=
ENST00000380743.8:c.835-78A=	ENSP00000370119.4:n.835-78A=
ENST00000505346.5:n.301-78A=
ENST00000506734.5:c.*59-576A=	ENSP00000424799.1:n.*59-576A=
ENST00000507458.2:c.89-78A=
ENST00000511812.5:c.634-78A=	ENSP00000424282.1:n.634-78A=
ENST00000514914.1:n.376-78A=
ENST00000614240.4:c.739-78A=	ENSP00000479279.1:n.739-78A=
ENST00000626847.2:c.835-576A=	ENSP00000486152.1:n.835-576A=
NM_017411.3:c.835-78A=	NP_059107.1:n.835-78A=
NM_022875.2:c.835-576A=	NP_075013.1:n.835-576A=
NM_022876.2:c.739-78A=	NP_075014.1:n.739-78A=
NM_022877.2:c.739-576A=	NP_075015.1:n.739-576A=
XM_011543600.1:c.634-78A=	XP_011541902.1:n.634-78A=
XM_011543601.1:c.634-576A=	XP_011541903.1:n.634-576A=
XM_011543602.1:c.538-78A=	XP_011541904.1:n.538-78A=
XM_011543603.1:c.538-576A=	XP_011541905.1:n.538-576A=
XR_948432.1:n.1054+88439A=
XM_011543600.2:c.634-78A=	XP_011541902.1:n.634-78A=
XM_011543602.3:c.538-78A=	XP_011541904.1:n.538-78A=
XM_011543603.3:c.538-576A=	XP_011541905.1:n.538-576A=
NM_017411.4:c.835-78A= MANE Select	NP_059107.1:n.835-78A=
NM_022875.3:c.835-576A=	NP_075013.1:n.835-576A=