Canonical Allele Identifier: CA1554044450
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70076934C= , CM000667.2:g.70076934C= GRCh38
NC_000005.9:g.69372761C= , CM000667.1:g.69372761C= GRCh37
NC_000005.8:g.69408517C= NCBI36
NG_008728.1:g.32412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380743.9:c.*4-85C= MANE Select ENSP00000370119.4:n.*4-85C=
ENST00000380742.8:c.*4-85C= ENSP00000370118.4:n.*4-85C=
ENST00000380743.8:c.*4-85C= ENSP00000370119.4:n.*4-85C=
ENST00000506734.5:c.*59-85C= ENSP00000424799.1:n.*59-85C=
ENST00000507458.2:c.143-85C=
ENST00000514914.1:n.430-85C=
ENST00000626847.2:c.835-85C= ENSP00000486152.1:n.835-85C=
NM_017411.3:c.*4-85C= NP_059107.1:n.*4-85C=
NM_022875.2:c.835-85C= NP_075013.1:n.835-85C=
NM_022876.2:c.*4-85C= NP_075014.1:n.*4-85C=
NM_022877.2:c.739-85C= NP_075015.1:n.739-85C=
XM_011543600.1:c.*4-85C= XP_011541902.1:n.*4-85C=
XM_011543601.1:c.634-85C= XP_011541903.1:n.634-85C=
XM_011543602.1:c.*4-85C= XP_011541904.1:n.*4-85C=
XM_011543603.1:c.538-85C= XP_011541905.1:n.538-85C=
XR_948432.1:n.1054+88930C=
XM_011543600.2:c.*4-85C= XP_011541902.1:n.*4-85C=
XM_011543602.3:c.*4-85C= XP_011541904.1:n.*4-85C=
XM_011543603.3:c.538-85C= XP_011541905.1:n.538-85C=
NM_017411.4:c.*4-85C= MANE Select NP_059107.1:n.*4-85C=
NM_022875.3:c.835-85C= NP_075013.1:n.835-85C=