Canonical Allele Identifier: CA360098267
Gene: SMN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70951959A>G , CM000667.2:g.70951959A>G GRCh38
NC_000005.9:g.70247786A>G , CM000667.1:g.70247786A>G GRCh37
NC_000005.8:g.70283542A>G NCBI36
NG_008691.1:g.32019A>G , LRG_676:g.32019A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380707.9:c.853A>G MANE Select ENSP00000370083.4:p.Lys285Glu
ENST00000351205.8:c.853A>G ENSP00000305857.5:p.Lys285Glu
ENST00000380707.8:c.853A>G ENSP00000370083.4:p.Lys285Glu
ENST00000503079.6:c.757A>G ENSP00000428128.1:p.Lys253Glu
ENST00000506163.5:c.835-480A>G ENSP00000424926.1:n.835-480A>G
ENST00000506239.6:c.*59-480A>G ENSP00000422679.2:n.*59-480A>G
ENST00000510679.1:n.107A>G
ENST00000514951.5:c.652A>G ENSP00000423298.1:p.Lys218Glu
NM_000344.3:c.853A>G , LRG_676t1:c.853A>G NP_000335.1:p.Lys285Glu
NM_001297715.1:c.835-480A>G NP_001284644.1:n.835-480A>G
NM_022874.2:c.757A>G NP_075012.1:p.Lys253Glu
XM_011543597.1:c.652A>G XP_011541899.1:p.Lys218Glu
XM_011543598.1:c.556A>G XP_011541900.1:p.Lys186Glu
XM_011543598.3:c.556A>G XP_011541900.1:p.Lys186Glu
XM_017009786.1:c.739-480A>G XP_016865275.1:n.739-480A>G
NM_000344.4:c.853A>G MANE Select NP_000335.1:p.Lys285Glu