Canonical Allele Identifier: CA1246138938
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022376_39022377delinsTA , CM000664.2:g.39022376_39022377delinsTA GRCh38
NC_000002.11:g.39249517_39249518delinsTA , CM000664.1:g.39249517_39249518delinsTA GRCh37
NC_000002.10:g.39103021_39103022delinsTA NCBI36
NG_007530.1:g.103087_103088delinsTA , LRG_754:g.103087_103088delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1931_1932delinsTA
ENST00000685279.1:c.625+193_625+194delinsTA ENSP00000509424.1:n.625+193_625+194delinsTA
ENST00000688043.1:n.2079+193_2079+194delinsTA
ENST00000689668.1:n.1865+193_1865+194delinsTA
ENST00000690876.1:c.1747+193_1747+194delinsTA ENSP00000508955.1:n.1747+193_1747+194delinsTA
ENST00000691229.1:c.1747+193_1747+194delinsTA ENSP00000510437.1:n.1747+193_1747+194delinsTA
ENST00000692089.1:c.1747+193_1747+194delinsTA ENSP00000508626.1:n.1747+193_1747+194delinsTA
ENST00000692620.1:c.625+193_625+194delinsTA ENSP00000509311.1:n.625+193_625+194delinsTA
ENST00000402219.8:c.1858+193_1858+194delinsTA MANE Select ENSP00000384675.2:n.1858+193_1858+194delinsTA
ENST00000395038.6:c.1858+193_1858+194delinsTA ENSP00000378479.2:n.1858+193_1858+194delinsTA
ENST00000402219.6:c.1858+193_1858+194delinsTA ENSP00000384675.2:n.1858+193_1858+194delinsTA
ENST00000426016.5:c.1858+193_1858+194delinsTA ENSP00000387784.1:n.1858+193_1858+194delinsTA
NM_005633.3:c.1858+193_1858+194delinsTA , LRG_754t1:c.1858+193_1858+194delinsTA NP_005624.2:n.1858+193_1858+194delinsTA
XM_005264515.3:c.1858+193_1858+194delinsTA XP_005264572.1:n.1858+193_1858+194delinsTA
XM_011533060.1:c.1951+193_1951+194delinsTA XP_011531362.1:n.1951+193_1951+194delinsTA
XM_011533061.1:c.1951+193_1951+194delinsTA XP_011531363.1:n.1951+193_1951+194delinsTA
XM_011533062.1:c.1837+193_1837+194delinsTA XP_011531364.1:n.1837+193_1837+194delinsTA
XM_011533063.1:c.1834+193_1834+194delinsTA XP_011531365.1:n.1834+193_1834+194delinsTA
XM_011533064.1:c.1687+193_1687+194delinsTA XP_011531366.1:n.1687+193_1687+194delinsTA
XM_011533065.1:c.1951+193_1951+194delinsTA XP_011531367.1:n.1951+193_1951+194delinsTA
XM_011533066.1:c.793+193_793+194delinsTA XP_011531368.1:n.793+193_793+194delinsTA
XM_005264515.4:c.1858+193_1858+194delinsTA XP_005264572.1:n.1858+193_1858+194delinsTA
XM_011533062.2:c.1837+193_1837+194delinsTA XP_011531364.1:n.1837+193_1837+194delinsTA
XM_011533064.2:c.1687+193_1687+194delinsTA XP_011531366.1:n.1687+193_1687+194delinsTA
NM_001382394.1:c.1837+193_1837+194delinsTA NP_001369323.1:n.1837+193_1837+194delinsTA
NM_001382395.1:c.1858+193_1858+194delinsTA NP_001369324.1:n.1858+193_1858+194delinsTA
NM_005633.4:c.1858+193_1858+194delinsTA MANE Select NP_005624.2:n.1858+193_1858+194delinsTA