Canonical Allele Identifier: CA1246139265
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022655G= , CM000664.2:g.39022655G= GRCh38
NC_000002.11:g.39249796G= , CM000664.1:g.39249796G= GRCh37
NC_000002.10:g.39103300G= NCBI36
NG_007530.1:g.102809C= , LRG_754:g.102809C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1653C=
ENST00000685279.1:c.540C= ENSP00000509424.1:p.Asn180=
ENST00000688043.1:n.1994C=
ENST00000689668.1:n.1780C=
ENST00000690876.1:c.1662C= ENSP00000508955.1:p.Asn554=
ENST00000691229.1:c.1662C= ENSP00000510437.1:p.Asn554=
ENST00000692089.1:c.1662C= ENSP00000508626.1:p.Asn554=
ENST00000692620.1:c.540C= ENSP00000509311.1:p.Asn180=
ENST00000402219.8:c.1773C= MANE Select ENSP00000384675.2:p.Asn591=
ENST00000395038.6:c.1773C= ENSP00000378479.2:p.Asn591=
ENST00000402219.6:c.1773C= ENSP00000384675.2:p.Asn591=
ENST00000426016.5:c.1773C= ENSP00000387784.1:p.Asn591=
NM_005633.3:c.1773C= , LRG_754t1:c.1773C= NP_005624.2:p.Asn591=
XM_005264515.3:c.1773C= XP_005264572.1:p.Asn591=
XM_011533060.1:c.1866C= XP_011531362.1:p.Asn622=
XM_011533061.1:c.1866C= XP_011531363.1:p.Asn622=
XM_011533062.1:c.1752C= XP_011531364.1:p.Asn584=
XM_011533063.1:c.1749C= XP_011531365.1:p.Asn583=
XM_011533064.1:c.1602C= XP_011531366.1:p.Asn534=
XM_011533065.1:c.1866C= XP_011531367.1:p.Asn622=
XM_011533066.1:c.708C= XP_011531368.1:p.Asn236=
XM_005264515.4:c.1773C= XP_005264572.1:p.Asn591=
XM_011533062.2:c.1752C= XP_011531364.1:p.Asn584=
XM_011533064.2:c.1602C= XP_011531366.1:p.Asn534=
NM_001382394.1:c.1752C= NP_001369323.1:p.Asn584=
NM_001382395.1:c.1773C= NP_001369324.1:p.Asn591=
NM_005633.4:c.1773C= MANE Select NP_005624.2:p.Asn591=
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