Canonical Allele Identifier: CA1246139205
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022613A= , CM000664.2:g.39022613A= GRCh38
NC_000002.11:g.39249754A= , CM000664.1:g.39249754A= GRCh37
NC_000002.10:g.39103258A= NCBI36
NG_007530.1:g.102851T= , LRG_754:g.102851T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1695T=
ENST00000685279.1:c.582T= ENSP00000509424.1:p.Thr194=
ENST00000688043.1:n.2036T=
ENST00000689668.1:n.1822T=
ENST00000690876.1:c.1704T= ENSP00000508955.1:p.Thr568=
ENST00000691229.1:c.1704T= ENSP00000510437.1:p.Thr568=
ENST00000692089.1:c.1704T= ENSP00000508626.1:p.Thr568=
ENST00000692620.1:c.582T= ENSP00000509311.1:p.Thr194=
ENST00000402219.8:c.1815T= MANE Select ENSP00000384675.2:p.Thr605=
ENST00000395038.6:c.1815T= ENSP00000378479.2:p.Thr605=
ENST00000402219.6:c.1815T= ENSP00000384675.2:p.Thr605=
ENST00000426016.5:c.1815T= ENSP00000387784.1:p.Thr605=
NM_005633.3:c.1815T= , LRG_754t1:c.1815T= NP_005624.2:p.Thr605=
XM_005264515.3:c.1815T= XP_005264572.1:p.Thr605=
XM_011533060.1:c.1908T= XP_011531362.1:p.Thr636=
XM_011533061.1:c.1908T= XP_011531363.1:p.Thr636=
XM_011533062.1:c.1794T= XP_011531364.1:p.Thr598=
XM_011533063.1:c.1791T= XP_011531365.1:p.Thr597=
XM_011533064.1:c.1644T= XP_011531366.1:p.Thr548=
XM_011533065.1:c.1908T= XP_011531367.1:p.Thr636=
XM_011533066.1:c.750T= XP_011531368.1:p.Thr250=
XM_005264515.4:c.1815T= XP_005264572.1:p.Thr605=
XM_011533062.2:c.1794T= XP_011531364.1:p.Thr598=
XM_011533064.2:c.1644T= XP_011531366.1:p.Thr548=
NM_001382394.1:c.1794T= NP_001369323.1:p.Thr598=
NM_001382395.1:c.1815T= NP_001369324.1:p.Thr605=
NM_005633.4:c.1815T= MANE Select NP_005624.2:p.Thr605=
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