Canonical Allele Identifier: CA1554042303

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070506_70070507delinsGA , CM000667.2:g.70070506_70070507delinsGA	GRCh38
NC_000005.9:g.69366333_69366334delinsGA , CM000667.1:g.69366333_69366334delinsGA	GRCh37
NC_000005.8:g.69402089_69402090delinsGA	NCBI36
NG_008728.1:g.25984_25985delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.724-135_724-134delinsGA MANE Select	ENSP00000370119.4:n.724-135_724-134delinsGA
ENST00000638794.1:c.724-135_724-134delinsGA	ENSP00000492675.1:n.724-135_724-134delinsGA
ENST00000380741.8:c.724-135_724-134delinsGA	ENSP00000370117.5:n.724-135_724-134delinsGA
ENST00000380742.8:c.628-135_628-134delinsGA	ENSP00000370118.4:n.628-135_628-134delinsGA
ENST00000380743.8:c.724-135_724-134delinsGA	ENSP00000370119.4:n.724-135_724-134delinsGA
ENST00000503678.5:n.647-135_647-134delinsGA
ENST00000505346.5:n.190-135_190-134delinsGA
ENST00000506734.5:c.724-135_724-134delinsGA	ENSP00000424799.1:n.724-135_724-134delinsGA
ENST00000508258.1:n.99-135_99-134delinsGA
ENST00000509805.5:n.291-135_291-134delinsGA
ENST00000511812.5:c.523-135_523-134delinsGA	ENSP00000424282.1:n.523-135_523-134delinsGA
ENST00000511873.6:c.418-135_418-134delinsGA	ENSP00000475824.1:n.418-135_418-134delinsGA
ENST00000514914.1:n.265-135_265-134delinsGA
ENST00000614240.4:c.628-135_628-134delinsGA	ENSP00000479279.1:n.628-135_628-134delinsGA
ENST00000626847.2:c.724-135_724-134delinsGA	ENSP00000486152.1:n.724-135_724-134delinsGA
ENST00000628696.2:c.724-135_724-134delinsGA	ENSP00000486268.1:n.724-135_724-134delinsGA
NM_017411.3:c.724-135_724-134delinsGA	NP_059107.1:n.724-135_724-134delinsGA
NM_022875.2:c.724-135_724-134delinsGA	NP_075013.1:n.724-135_724-134delinsGA
NM_022876.2:c.628-135_628-134delinsGA	NP_075014.1:n.628-135_628-134delinsGA
NM_022877.2:c.628-135_628-134delinsGA	NP_075015.1:n.628-135_628-134delinsGA
XM_011543599.1:c.724-135_724-134delinsGA	XP_011541901.1:n.724-135_724-134delinsGA
XM_011543600.1:c.523-135_523-134delinsGA	XP_011541902.1:n.523-135_523-134delinsGA
XM_011543601.1:c.523-135_523-134delinsGA	XP_011541903.1:n.523-135_523-134delinsGA
XM_011543602.1:c.427-135_427-134delinsGA	XP_011541904.1:n.427-135_427-134delinsGA
XM_011543603.1:c.427-135_427-134delinsGA	XP_011541905.1:n.427-135_427-134delinsGA
XR_948432.1:n.1054+82502_1054+82503delinsGA
XM_011543600.2:c.523-135_523-134delinsGA	XP_011541902.1:n.523-135_523-134delinsGA
XM_011543602.3:c.427-135_427-134delinsGA	XP_011541904.1:n.427-135_427-134delinsGA
XM_011543603.3:c.427-135_427-134delinsGA	XP_011541905.1:n.427-135_427-134delinsGA
XM_017009787.1:c.724-135_724-134delinsGA	XP_016865276.1:n.724-135_724-134delinsGA
NM_017411.4:c.724-135_724-134delinsGA MANE Select	NP_059107.1:n.724-135_724-134delinsGA
NM_022875.3:c.724-135_724-134delinsGA	NP_075013.1:n.724-135_724-134delinsGA