Canonical Allele Identifier: CA1246139628
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022844G= , CM000664.2:g.39022844G= GRCh38
NC_000002.11:g.39249985G= , CM000664.1:g.39249985G= GRCh37
NC_000002.10:g.39103489G= NCBI36
NG_007530.1:g.102620C= , LRG_754:g.102620C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1464C=
ENST00000685279.1:c.351C= ENSP00000509424.1:p.Ala117=
ENST00000688043.1:n.1805C=
ENST00000689668.1:n.1591C=
ENST00000690876.1:c.1473C= ENSP00000508955.1:p.Ala491=
ENST00000691229.1:c.1473C= ENSP00000510437.1:p.Ala491=
ENST00000692089.1:c.1473C= ENSP00000508626.1:p.Ala491=
ENST00000692620.1:c.351C= ENSP00000509311.1:p.Ala117=
ENST00000402219.8:c.1584C= MANE Select ENSP00000384675.2:p.Ala528=
ENST00000395038.6:c.1584C= ENSP00000378479.2:p.Ala528=
ENST00000402219.6:c.1584C= ENSP00000384675.2:p.Ala528=
ENST00000426016.5:c.1584C= ENSP00000387784.1:p.Ala528=
NM_005633.3:c.1584C= , LRG_754t1:c.1584C= NP_005624.2:p.Ala528=
XM_005264515.3:c.1584C= XP_005264572.1:p.Ala528=
XM_011533060.1:c.1677C= XP_011531362.1:p.Ala559=
XM_011533061.1:c.1677C= XP_011531363.1:p.Ala559=
XM_011533062.1:c.1563C= XP_011531364.1:p.Ala521=
XM_011533063.1:c.1560C= XP_011531365.1:p.Ala520=
XM_011533064.1:c.1413C= XP_011531366.1:p.Ala471=
XM_011533065.1:c.1677C= XP_011531367.1:p.Ala559=
XM_011533066.1:c.519C= XP_011531368.1:p.Ala173=
XM_005264515.4:c.1584C= XP_005264572.1:p.Ala528=
XM_011533062.2:c.1563C= XP_011531364.1:p.Ala521=
XM_011533064.2:c.1413C= XP_011531366.1:p.Ala471=
NM_001382394.1:c.1563C= NP_001369323.1:p.Ala521=
NM_001382395.1:c.1584C= NP_001369324.1:p.Ala528=
NM_005633.4:c.1584C= MANE Select NP_005624.2:p.Ala528=
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