Canonical Allele Identifier: CA1554042304

Gene: SMN2

Linked Data

• dbSNP Id: rs1247448005
• gnomAD v4: 5-70070506-G-GA

Genomic Alleles

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

Transcript Alleles

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