Canonical Allele Identifier: CA1246139655
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022862A= , CM000664.2:g.39022862A= GRCh38
NC_000002.11:g.39250003A= , CM000664.1:g.39250003A= GRCh37
NC_000002.10:g.39103507A= NCBI36
NG_007530.1:g.102602T= , LRG_754:g.102602T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1446T=
ENST00000685279.1:c.333T= ENSP00000509424.1:p.Asn111=
ENST00000688043.1:n.1787T=
ENST00000689668.1:n.1573T=
ENST00000690876.1:c.1455T= ENSP00000508955.1:p.Asn485=
ENST00000691229.1:c.1455T= ENSP00000510437.1:p.Asn485=
ENST00000692089.1:c.1455T= ENSP00000508626.1:p.Asn485=
ENST00000692620.1:c.333T= ENSP00000509311.1:p.Asn111=
ENST00000402219.8:c.1566T= MANE Select ENSP00000384675.2:p.Asn522=
ENST00000395038.6:c.1566T= ENSP00000378479.2:p.Asn522=
ENST00000402219.6:c.1566T= ENSP00000384675.2:p.Asn522=
ENST00000426016.5:c.1566T= ENSP00000387784.1:p.Asn522=
NM_005633.3:c.1566T= , LRG_754t1:c.1566T= NP_005624.2:p.Asn522=
XM_005264515.3:c.1566T= XP_005264572.1:p.Asn522=
XM_011533060.1:c.1659T= XP_011531362.1:p.Asn553=
XM_011533061.1:c.1659T= XP_011531363.1:p.Asn553=
XM_011533062.1:c.1545T= XP_011531364.1:p.Asn515=
XM_011533063.1:c.1542T= XP_011531365.1:p.Asn514=
XM_011533064.1:c.1395T= XP_011531366.1:p.Asn465=
XM_011533065.1:c.1659T= XP_011531367.1:p.Asn553=
XM_011533066.1:c.501T= XP_011531368.1:p.Asn167=
XM_005264515.4:c.1566T= XP_005264572.1:p.Asn522=
XM_011533062.2:c.1545T= XP_011531364.1:p.Asn515=
XM_011533064.2:c.1395T= XP_011531366.1:p.Asn465=
NM_001382394.1:c.1545T= NP_001369323.1:p.Asn515=
NM_001382395.1:c.1566T= NP_001369324.1:p.Asn522=
NM_005633.4:c.1566T= MANE Select NP_005624.2:p.Asn522=
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