Canonical Allele Identifier: CA360086139

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69366470A>G (hg19) ; chr5:g.70070643A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070643A>G , CM000667.2:g.70070643A>G	GRCh38
NC_000005.9:g.69366470A>G , CM000667.1:g.69366470A>G	GRCh37
NC_000005.8:g.69402226A>G	NCBI36
NG_008728.1:g.26121A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380743.9:c.726A>G MANE Select	ENSP00000370119.4:p.Ile242Met
ENST00000638794.1:c.726A>G	ENSP00000492675.1:p.Ile242Met
ENST00000380741.8:c.726A>G	ENSP00000370117.5:p.Ile242Met
ENST00000380742.8:c.630A>G	ENSP00000370118.4:p.Ile210Met
ENST00000380743.8:c.726A>G	ENSP00000370119.4:p.Ile242Met
ENST00000503678.5:n.649A>G
ENST00000505346.5:n.192A>G
ENST00000506734.5:c.726A>G	ENSP00000424799.1:p.Ile242Met
ENST00000508258.1:n.101A>G
ENST00000509805.5:n.293A>G
ENST00000511812.5:c.525A>G	ENSP00000424282.1:p.Ile175Met
ENST00000511873.6:c.420A>G	ENSP00000475824.1:n.420A>G
ENST00000514914.1:n.267A>G
ENST00000614240.4:c.630A>G	ENSP00000479279.1:p.Ile210Met
ENST00000626847.2:c.726A>G	ENSP00000486152.1:p.Ile242Met
ENST00000628696.2:c.726A>G	ENSP00000486268.1:p.Ile242Met
NM_017411.3:c.726A>G	NP_059107.1:p.Ile242Met
NM_022875.2:c.726A>G	NP_075013.1:p.Ile242Met
NM_022876.2:c.630A>G	NP_075014.1:p.Ile210Met
NM_022877.2:c.630A>G	NP_075015.1:p.Ile210Met
XM_011543599.1:c.726A>G	XP_011541901.1:p.Ile242Met
XM_011543600.1:c.525A>G	XP_011541902.1:p.Ile175Met
XM_011543601.1:c.525A>G	XP_011541903.1:p.Ile175Met
XM_011543602.1:c.429A>G	XP_011541904.1:p.Ile143Met
XM_011543603.1:c.429A>G	XP_011541905.1:p.Ile143Met
XR_948432.1:n.1054+82639A>G
XM_011543600.2:c.525A>G	XP_011541902.1:p.Ile175Met
XM_011543602.3:c.429A>G	XP_011541904.1:p.Ile143Met
XM_011543603.3:c.429A>G	XP_011541905.1:p.Ile143Met
XM_017009787.1:c.726A>G	XP_016865276.1:p.Ile242Met
NM_017411.4:c.726A>G MANE Select	NP_059107.1:p.Ile242Met
NM_022875.3:c.726A>G	NP_075013.1:p.Ile242Met