Canonical Allele Identifier: CA1554044348

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076586A= , CM000667.2:g.70076586A=	GRCh38
NC_000005.9:g.69372413A= , CM000667.1:g.69372413A=	GRCh37
NC_000005.8:g.69408169A=	NCBI36
NG_008728.1:g.32064A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.*3+12A= MANE Select	ENSP00000370119.4:n.*3+12A=
ENST00000380741.8:c.900A=	ENSP00000370117.5:n.900A=
ENST00000380742.8:c.*3+12A=	ENSP00000370118.4:n.*3+12A=
ENST00000380743.8:c.*3+12A=	ENSP00000370119.4:n.*3+12A=
ENST00000505346.5:n.366A=
ENST00000506734.5:c.*59-433A=	ENSP00000424799.1:n.*59-433A=
ENST00000507458.2:c.142+12A=
ENST00000511812.5:c.*15A=	ENSP00000424282.1:n.*15A=
ENST00000514914.1:n.429+12A=
ENST00000614240.4:c.804A=	ENSP00000479279.1:n.804A=
ENST00000626847.2:c.835-433A=	ENSP00000486152.1:n.835-433A=
NM_017411.3:c.*3+12A=	NP_059107.1:n.*3+12A=
NM_022875.2:c.835-433A=	NP_075013.1:n.835-433A=
NM_022876.2:c.*3+12A=	NP_075014.1:n.*3+12A=
NM_022877.2:c.739-433A=	NP_075015.1:n.739-433A=
XM_011543600.1:c.*3+12A=	XP_011541902.1:n.*3+12A=
XM_011543601.1:c.634-433A=	XP_011541903.1:n.634-433A=
XM_011543602.1:c.*3+12A=	XP_011541904.1:n.*3+12A=
XM_011543603.1:c.538-433A=	XP_011541905.1:n.538-433A=
XR_948432.1:n.1054+88582A=
XM_011543600.2:c.*3+12A=	XP_011541902.1:n.*3+12A=
XM_011543602.3:c.*3+12A=	XP_011541904.1:n.*3+12A=
XM_011543603.3:c.538-433A=	XP_011541905.1:n.538-433A=
NM_017411.4:c.*3+12A= MANE Select	NP_059107.1:n.*3+12A=
NM_022875.3:c.835-433A=	NP_075013.1:n.835-433A=