Canonical Allele Identifier: CA444901711

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69372365A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076538A>G , CM000667.2:g.70076538A>G	GRCh38
NC_000005.9:g.69372365A>G , CM000667.1:g.69372365A>G	GRCh37
NC_000005.8:g.69408121A>G	NCBI36
NG_008728.1:g.32016A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.852A>G MANE Select	ENSP00000370119.4:p.Gln284=
ENST00000380741.8:c.852A>G	ENSP00000370117.5:p.Gln284=
ENST00000380742.8:c.756A>G	ENSP00000370118.4:p.Gln252=
ENST00000380743.8:c.852A>G	ENSP00000370119.4:p.Gln284=
ENST00000505346.5:n.318A>G
ENST00000506734.5:c.*59-481A>G	ENSP00000424799.1:n.*59-481A>G
ENST00000507458.2:c.106A>G
ENST00000511812.5:c.651A>G	ENSP00000424282.1:p.Gln217=
ENST00000514914.1:n.393A>G
ENST00000614240.4:c.756A>G	ENSP00000479279.1:p.Gln252=
ENST00000626847.2:c.835-481A>G	ENSP00000486152.1:n.835-481A>G
NM_017411.3:c.852A>G	NP_059107.1:p.Gln284=
NM_022875.2:c.835-481A>G	NP_075013.1:n.835-481A>G
NM_022876.2:c.756A>G	NP_075014.1:p.Gln252=
NM_022877.2:c.739-481A>G	NP_075015.1:n.739-481A>G
XM_011543600.1:c.651A>G	XP_011541902.1:p.Gln217=
XM_011543601.1:c.634-481A>G	XP_011541903.1:n.634-481A>G
XM_011543602.1:c.555A>G	XP_011541904.1:p.Gln185=
XM_011543603.1:c.538-481A>G	XP_011541905.1:n.538-481A>G
XR_948432.1:n.1054+88534A>G
XM_011543600.2:c.651A>G	XP_011541902.1:p.Gln217=
XM_011543602.3:c.555A>G	XP_011541904.1:p.Gln185=
XM_011543603.3:c.538-481A>G	XP_011541905.1:n.538-481A>G
NM_017411.4:c.852A>G MANE Select	NP_059107.1:p.Gln284=
NM_022875.3:c.835-481A>G	NP_075013.1:n.835-481A>G