Canonical Allele Identifier: CA1554041041
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1774432698

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049700dup , CM000667.2:g.70049700dup GRCh38
NC_000005.9:g.69345527dup , CM000667.1:g.69345527dup GRCh37
NC_000005.8:g.69381283dup NCBI36
NG_008728.1:g.5178dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380743.9:c.15dup MANE Select ENSP00000370119.4:p.Gly6ArgfsTer25
ENST00000638794.1:c.15dup ENSP00000492675.1:p.Gly6ArgfsTer25
ENST00000380741.8:c.15dup ENSP00000370117.5:p.Gly6ArgfsTer25
ENST00000380742.8:c.15dup ENSP00000370118.4:p.Gly6ArgfsTer25
ENST00000380743.8:c.15dup ENSP00000370119.4:p.Gly6ArgfsTer25
ENST00000506734.5:c.15dup ENSP00000424799.1:p.Gly6ArgfsTer25
ENST00000511812.5:c.15dup ENSP00000424282.1:p.Gly6ArgfsTer25
ENST00000614240.4:c.15dup ENSP00000479279.1:p.Gly6ArgfsTer25
ENST00000626847.2:c.15dup ENSP00000486152.1:p.Gly6ArgfsTer25
ENST00000628696.2:c.15dup ENSP00000486268.1:p.Gly6ArgfsTer25
NM_017411.3:c.15dup NP_059107.1:p.Gly6ArgfsTer25
NM_022875.2:c.15dup NP_075013.1:p.Gly6ArgfsTer25
NM_022876.2:c.15dup NP_075014.1:p.Gly6ArgfsTer25
NM_022877.2:c.15dup NP_075015.1:p.Gly6ArgfsTer25
XM_011543599.1:c.15dup XP_011541901.1:p.Gly6ArgfsTer25
XM_011543600.1:c.15dup XP_011541902.1:p.Gly6ArgfsTer25
XM_011543601.1:c.15dup XP_011541903.1:p.Gly6ArgfsTer25
XM_011543602.1:c.15dup XP_011541904.1:p.Gly6ArgfsTer25
XM_011543603.1:c.15dup XP_011541905.1:p.Gly6ArgfsTer25
XR_948432.1:n.1054+61696dup
XM_011543600.2:c.15dup XP_011541902.1:p.Gly6ArgfsTer25
XM_011543602.3:c.15dup XP_011541904.1:p.Gly6ArgfsTer25
XM_011543603.3:c.15dup XP_011541905.1:p.Gly6ArgfsTer25
XM_017009787.1:c.15dup XP_016865276.1:p.Gly6ArgfsTer25
NM_017411.4:c.15dup MANE Select NP_059107.1:p.Gly6ArgfsTer25
NM_022875.3:c.15dup NP_075013.1:p.Gly6ArgfsTer25