Canonical Allele Identifier: CA1554042308

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070514A= , CM000667.2:g.70070514A=	GRCh38
NC_000005.9:g.69366341A= , CM000667.1:g.69366341A=	GRCh37
NC_000005.8:g.69402097A=	NCBI36
NG_008728.1:g.25992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.724-127A= MANE Select	ENSP00000370119.4:n.724-127A=
ENST00000638794.1:c.724-127A=	ENSP00000492675.1:n.724-127A=
ENST00000380741.8:c.724-127A=	ENSP00000370117.5:n.724-127A=
ENST00000380742.8:c.628-127A=	ENSP00000370118.4:n.628-127A=
ENST00000380743.8:c.724-127A=	ENSP00000370119.4:n.724-127A=
ENST00000503678.5:n.647-127A=
ENST00000505346.5:n.190-127A=
ENST00000506734.5:c.724-127A=	ENSP00000424799.1:n.724-127A=
ENST00000508258.1:n.99-127A=
ENST00000509805.5:n.291-127A=
ENST00000511812.5:c.523-127A=	ENSP00000424282.1:n.523-127A=
ENST00000511873.6:c.418-127A=	ENSP00000475824.1:n.418-127A=
ENST00000514914.1:n.265-127A=
ENST00000614240.4:c.628-127A=	ENSP00000479279.1:n.628-127A=
ENST00000626847.2:c.724-127A=	ENSP00000486152.1:n.724-127A=
ENST00000628696.2:c.724-127A=	ENSP00000486268.1:n.724-127A=
NM_017411.3:c.724-127A=	NP_059107.1:n.724-127A=
NM_022875.2:c.724-127A=	NP_075013.1:n.724-127A=
NM_022876.2:c.628-127A=	NP_075014.1:n.628-127A=
NM_022877.2:c.628-127A=	NP_075015.1:n.628-127A=
XM_011543599.1:c.724-127A=	XP_011541901.1:n.724-127A=
XM_011543600.1:c.523-127A=	XP_011541902.1:n.523-127A=
XM_011543601.1:c.523-127A=	XP_011541903.1:n.523-127A=
XM_011543602.1:c.427-127A=	XP_011541904.1:n.427-127A=
XM_011543603.1:c.427-127A=	XP_011541905.1:n.427-127A=
XR_948432.1:n.1054+82510A=
XM_011543600.2:c.523-127A=	XP_011541902.1:n.523-127A=
XM_011543602.3:c.427-127A=	XP_011541904.1:n.427-127A=
XM_011543603.3:c.427-127A=	XP_011541905.1:n.427-127A=
XM_017009787.1:c.724-127A=	XP_016865276.1:n.724-127A=
NM_017411.4:c.724-127A= MANE Select	NP_059107.1:n.724-127A=
NM_022875.3:c.724-127A=	NP_075013.1:n.724-127A=