Canonical Allele Identifier: CA2514686833
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022530del , CM000664.2:g.39022530del GRCh38
NC_000002.11:g.39249671del , CM000664.1:g.39249671del GRCh37
NC_000002.10:g.39103175del NCBI36
NG_007530.1:g.102934del , LRG_754:g.102934del

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1778del
ENST00000685279.1:c.625+40del ENSP00000509424.1:n.625+40del
ENST00000688043.1:n.2079+40del
ENST00000689668.1:n.1865+40del
ENST00000690876.1:c.1747+40del ENSP00000508955.1:n.1747+40del
ENST00000691229.1:c.1747+40del ENSP00000510437.1:n.1747+40del
ENST00000692089.1:c.1747+40del ENSP00000508626.1:n.1747+40del
ENST00000692620.1:c.625+40del ENSP00000509311.1:n.625+40del
ENST00000402219.8:c.1858+40del MANE Select ENSP00000384675.2:n.1858+40del
ENST00000395038.6:c.1858+40del ENSP00000378479.2:n.1858+40del
ENST00000402219.6:c.1858+40del ENSP00000384675.2:n.1858+40del
ENST00000426016.5:c.1858+40del ENSP00000387784.1:n.1858+40del
NM_005633.3:c.1858+40del , LRG_754t1:c.1858+40del NP_005624.2:n.1858+40del
XM_005264515.3:c.1858+40del XP_005264572.1:n.1858+40del
XM_011533060.1:c.1951+40del XP_011531362.1:n.1951+40del
XM_011533061.1:c.1951+40del XP_011531363.1:n.1951+40del
XM_011533062.1:c.1837+40del XP_011531364.1:n.1837+40del
XM_011533063.1:c.1834+40del XP_011531365.1:n.1834+40del
XM_011533064.1:c.1687+40del XP_011531366.1:n.1687+40del
XM_011533065.1:c.1951+40del XP_011531367.1:n.1951+40del
XM_011533066.1:c.793+40del XP_011531368.1:n.793+40del
XM_005264515.4:c.1858+40del XP_005264572.1:n.1858+40del
XM_011533062.2:c.1837+40del XP_011531364.1:n.1837+40del
XM_011533064.2:c.1687+40del XP_011531366.1:n.1687+40del
NM_001382394.1:c.1837+40del NP_001369323.1:n.1837+40del
NM_001382395.1:c.1858+40del NP_001369324.1:n.1858+40del
NM_005633.4:c.1858+40del MANE Select NP_005624.2:n.1858+40del