Canonical Allele Identifier: CA1246153684
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054587G= , CM000664.2:g.39054587G= GRCh38
NC_000002.11:g.39281728G= , CM000664.1:g.39281728G= GRCh37
NC_000002.10:g.39135232G= NCBI36
NG_007530.1:g.70877C= , LRG_754:g.70877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.747+27C=
ENST00000685782.1:n.1558+27C=
ENST00000688189.1:n.512C=
ENST00000689668.1:n.727+27C=
ENST00000690679.1:c.820+27C=
ENST00000690876.1:c.720+27C= ENSP00000508955.1:n.720+27C=
ENST00000691229.1:c.720+27C= ENSP00000510437.1:n.720+27C=
ENST00000692089.1:c.720+27C= ENSP00000508626.1:n.720+27C=
ENST00000402219.8:c.720+27C= MANE Select ENSP00000384675.2:n.720+27C=
ENST00000395038.6:c.720+27C= ENSP00000378479.2:n.720+27C=
ENST00000402219.6:c.720+27C= ENSP00000384675.2:n.720+27C=
ENST00000426016.5:c.720+27C= ENSP00000387784.1:n.720+27C=
NM_005633.3:c.720+27C= , LRG_754t1:c.720+27C= NP_005624.2:n.720+27C=
XM_005264515.3:c.720+27C= XP_005264572.1:n.720+27C=
XM_011533060.1:c.813+27C= XP_011531362.1:n.813+27C=
XM_011533061.1:c.813+27C= XP_011531363.1:n.813+27C=
XM_011533062.1:c.699+27C= XP_011531364.1:n.699+27C=
XM_011533063.1:c.696+27C= XP_011531365.1:n.696+27C=
XM_011533064.1:c.549+27C= XP_011531366.1:n.549+27C=
XM_011533065.1:c.813+27C= XP_011531367.1:n.813+27C=
XM_005264515.4:c.720+27C= XP_005264572.1:n.720+27C=
XM_011533062.2:c.699+27C= XP_011531364.1:n.699+27C=
XM_011533064.2:c.549+27C= XP_011531366.1:n.549+27C=
NM_001382394.1:c.699+27C= NP_001369323.1:n.699+27C=
NM_001382395.1:c.720+27C= NP_001369324.1:n.720+27C=
NM_005633.4:c.720+27C= MANE Select NP_005624.2:n.720+27C=