Canonical Allele Identifier: CA2674142408

Gene: SMN2

Linked Data

• gnomAD v4: 5-70076756-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076756C>A , CM000667.2:g.70076756C>A	GRCh38
NC_000005.9:g.69372583C>A , CM000667.1:g.69372583C>A	GRCh37
NC_000005.8:g.69408339C>A	NCBI36
NG_008728.1:g.32234C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.*3+182C>A MANE Select	ENSP00000370119.4:n.*3+182C>A
ENST00000380742.8:c.*3+182C>A	ENSP00000370118.4:n.*3+182C>A
ENST00000380743.8:c.*3+182C>A	ENSP00000370119.4:n.*3+182C>A
ENST00000505346.5:n.536C>A
ENST00000506734.5:c.*59-263C>A	ENSP00000424799.1:n.*59-263C>A
ENST00000507458.2:c.142+182C>A
ENST00000514914.1:n.429+182C>A
ENST00000626847.2:c.835-263C>A	ENSP00000486152.1:n.835-263C>A
NM_017411.3:c.*3+182C>A	NP_059107.1:n.*3+182C>A
NM_022875.2:c.835-263C>A	NP_075013.1:n.835-263C>A
NM_022876.2:c.*3+182C>A	NP_075014.1:n.*3+182C>A
NM_022877.2:c.739-263C>A	NP_075015.1:n.739-263C>A
XM_011543600.1:c.*3+182C>A	XP_011541902.1:n.*3+182C>A
XM_011543601.1:c.634-263C>A	XP_011541903.1:n.634-263C>A
XM_011543602.1:c.*3+182C>A	XP_011541904.1:n.*3+182C>A
XM_011543603.1:c.538-263C>A	XP_011541905.1:n.538-263C>A
XR_948432.1:n.1054+88752C>A
XM_011543600.2:c.*3+182C>A	XP_011541902.1:n.*3+182C>A
XM_011543602.3:c.*3+182C>A	XP_011541904.1:n.*3+182C>A
XM_011543603.3:c.538-263C>A	XP_011541905.1:n.538-263C>A
NM_017411.4:c.*3+182C>A MANE Select	NP_059107.1:n.*3+182C>A
NM_022875.3:c.835-263C>A	NP_075013.1:n.835-263C>A