Canonical Allele Identifier: CA1246139613
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022820A= , CM000664.2:g.39022820A= GRCh38
NC_000002.11:g.39249961A= , CM000664.1:g.39249961A= GRCh37
NC_000002.10:g.39103465A= NCBI36
NG_007530.1:g.102644T= , LRG_754:g.102644T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1488T=
ENST00000685279.1:c.375T= ENSP00000509424.1:p.Asn125=
ENST00000688043.1:n.1829T=
ENST00000689668.1:n.1615T=
ENST00000690876.1:c.1497T= ENSP00000508955.1:p.Asn499=
ENST00000691229.1:c.1497T= ENSP00000510437.1:p.Asn499=
ENST00000692089.1:c.1497T= ENSP00000508626.1:p.Asn499=
ENST00000692620.1:c.375T= ENSP00000509311.1:p.Asn125=
ENST00000402219.8:c.1608T= MANE Select ENSP00000384675.2:p.Asn536=
ENST00000395038.6:c.1608T= ENSP00000378479.2:p.Asn536=
ENST00000402219.6:c.1608T= ENSP00000384675.2:p.Asn536=
ENST00000426016.5:c.1608T= ENSP00000387784.1:p.Asn536=
NM_005633.3:c.1608T= , LRG_754t1:c.1608T= NP_005624.2:p.Asn536=
XM_005264515.3:c.1608T= XP_005264572.1:p.Asn536=
XM_011533060.1:c.1701T= XP_011531362.1:p.Asn567=
XM_011533061.1:c.1701T= XP_011531363.1:p.Asn567=
XM_011533062.1:c.1587T= XP_011531364.1:p.Asn529=
XM_011533063.1:c.1584T= XP_011531365.1:p.Asn528=
XM_011533064.1:c.1437T= XP_011531366.1:p.Asn479=
XM_011533065.1:c.1701T= XP_011531367.1:p.Asn567=
XM_011533066.1:c.543T= XP_011531368.1:p.Asn181=
XM_005264515.4:c.1608T= XP_005264572.1:p.Asn536=
XM_011533062.2:c.1587T= XP_011531364.1:p.Asn529=
XM_011533064.2:c.1437T= XP_011531366.1:p.Asn479=
NM_001382394.1:c.1587T= NP_001369323.1:p.Asn529=
NM_001382395.1:c.1608T= NP_001369324.1:p.Asn536=
NM_005633.4:c.1608T= MANE Select NP_005624.2:p.Asn536=