Canonical Allele Identifier: CA2674142365

Gene: SMN2

Linked Data

• gnomAD v4: 5-70076663-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076663T>A , CM000667.2:g.70076663T>A	GRCh38
NC_000005.9:g.69372490T>A , CM000667.1:g.69372490T>A	GRCh37
NC_000005.8:g.69408246T>A	NCBI36
NG_008728.1:g.32141T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.*3+89T>A MANE Select	ENSP00000370119.4:n.*3+89T>A
ENST00000380742.8:c.*3+89T>A	ENSP00000370118.4:n.*3+89T>A
ENST00000380743.8:c.*3+89T>A	ENSP00000370119.4:n.*3+89T>A
ENST00000505346.5:n.443T>A
ENST00000506734.5:c.*59-356T>A	ENSP00000424799.1:n.*59-356T>A
ENST00000507458.2:c.142+89T>A
ENST00000511812.5:c.*92T>A	ENSP00000424282.1:n.*92T>A
ENST00000514914.1:n.429+89T>A
ENST00000626847.2:c.835-356T>A	ENSP00000486152.1:n.835-356T>A
NM_017411.3:c.*3+89T>A	NP_059107.1:n.*3+89T>A
NM_022875.2:c.835-356T>A	NP_075013.1:n.835-356T>A
NM_022876.2:c.*3+89T>A	NP_075014.1:n.*3+89T>A
NM_022877.2:c.739-356T>A	NP_075015.1:n.739-356T>A
XM_011543600.1:c.*3+89T>A	XP_011541902.1:n.*3+89T>A
XM_011543601.1:c.634-356T>A	XP_011541903.1:n.634-356T>A
XM_011543602.1:c.*3+89T>A	XP_011541904.1:n.*3+89T>A
XM_011543603.1:c.538-356T>A	XP_011541905.1:n.538-356T>A
XR_948432.1:n.1054+88659T>A
XM_011543600.2:c.*3+89T>A	XP_011541902.1:n.*3+89T>A
XM_011543602.3:c.*3+89T>A	XP_011541904.1:n.*3+89T>A
XM_011543603.3:c.538-356T>A	XP_011541905.1:n.538-356T>A
NM_017411.4:c.*3+89T>A MANE Select	NP_059107.1:n.*3+89T>A
NM_022875.3:c.835-356T>A	NP_075013.1:n.835-356T>A