Canonical Allele Identifier: CA444898551

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69366473T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070646T>A , CM000667.2:g.70070646T>A	GRCh38
NC_000005.9:g.69366473T>A , CM000667.1:g.69366473T>A	GRCh37
NC_000005.8:g.69402229T>A	NCBI36
NG_008728.1:g.26124T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380743.9:c.729T>A MANE Select	ENSP00000370119.4:p.Ile243=
ENST00000638794.1:c.729T>A	ENSP00000492675.1:p.Ile243=
ENST00000380741.8:c.729T>A	ENSP00000370117.5:p.Ile243=
ENST00000380742.8:c.633T>A	ENSP00000370118.4:p.Ile211=
ENST00000380743.8:c.729T>A	ENSP00000370119.4:p.Ile243=
ENST00000503678.5:n.652T>A
ENST00000505346.5:n.195T>A
ENST00000506734.5:c.729T>A	ENSP00000424799.1:p.Ile243=
ENST00000508258.1:n.104T>A
ENST00000509805.5:n.296T>A
ENST00000511812.5:c.528T>A	ENSP00000424282.1:p.Ile176=
ENST00000511873.6:c.423T>A	ENSP00000475824.1:n.423T>A
ENST00000514914.1:n.270T>A
ENST00000614240.4:c.633T>A	ENSP00000479279.1:p.Ile211=
ENST00000626847.2:c.729T>A	ENSP00000486152.1:p.Ile243=
ENST00000628696.2:c.729T>A	ENSP00000486268.1:p.Ile243=
NM_017411.3:c.729T>A	NP_059107.1:p.Ile243=
NM_022875.2:c.729T>A	NP_075013.1:p.Ile243=
NM_022876.2:c.633T>A	NP_075014.1:p.Ile211=
NM_022877.2:c.633T>A	NP_075015.1:p.Ile211=
XM_011543599.1:c.729T>A	XP_011541901.1:p.Ile243=
XM_011543600.1:c.528T>A	XP_011541902.1:p.Ile176=
XM_011543601.1:c.528T>A	XP_011541903.1:p.Ile176=
XM_011543602.1:c.432T>A	XP_011541904.1:p.Ile144=
XM_011543603.1:c.432T>A	XP_011541905.1:p.Ile144=
XR_948432.1:n.1054+82642T>A
XM_011543600.2:c.528T>A	XP_011541902.1:p.Ile176=
XM_011543602.3:c.432T>A	XP_011541904.1:p.Ile144=
XM_011543603.3:c.432T>A	XP_011541905.1:p.Ile144=
XM_017009787.1:c.729T>A	XP_016865276.1:p.Ile243=
NM_017411.4:c.729T>A MANE Select	NP_059107.1:p.Ile243=
NM_022875.3:c.729T>A	NP_075013.1:p.Ile243=