Canonical Allele Identifier: CA1246139649
Gene: SOS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022860C= , CM000664.2:g.39022860C= GRCh38
NC_000002.11:g.39250001C= , CM000664.1:g.39250001C= GRCh37
NC_000002.10:g.39103505C= NCBI36
NG_007530.1:g.102604G= , LRG_754:g.102604G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1448G=
ENST00000685279.1:c.335G= ENSP00000509424.1:p.Ser112=
ENST00000688043.1:n.1789G=
ENST00000689668.1:n.1575G=
ENST00000690876.1:c.1457G= ENSP00000508955.1:p.Ser486=
ENST00000691229.1:c.1457G= ENSP00000510437.1:p.Ser486=
ENST00000692089.1:c.1457G= ENSP00000508626.1:p.Ser486=
ENST00000692620.1:c.335G= ENSP00000509311.1:p.Ser112=
ENST00000402219.8:c.1568G= MANE Select ENSP00000384675.2:p.Ser523=
ENST00000395038.6:c.1568G= ENSP00000378479.2:p.Ser523=
ENST00000402219.6:c.1568G= ENSP00000384675.2:p.Ser523=
ENST00000426016.5:c.1568G= ENSP00000387784.1:p.Ser523=
NM_005633.3:c.1568G= , LRG_754t1:c.1568G= NP_005624.2:p.Ser523=
XM_005264515.3:c.1568G= XP_005264572.1:p.Ser523=
XM_011533060.1:c.1661G= XP_011531362.1:p.Ser554=
XM_011533061.1:c.1661G= XP_011531363.1:p.Ser554=
XM_011533062.1:c.1547G= XP_011531364.1:p.Ser516=
XM_011533063.1:c.1544G= XP_011531365.1:p.Ser515=
XM_011533064.1:c.1397G= XP_011531366.1:p.Ser466=
XM_011533065.1:c.1661G= XP_011531367.1:p.Ser554=
XM_011533066.1:c.503G= XP_011531368.1:p.Ser168=
XM_005264515.4:c.1568G= XP_005264572.1:p.Ser523=
XM_011533062.2:c.1547G= XP_011531364.1:p.Ser516=
XM_011533064.2:c.1397G= XP_011531366.1:p.Ser466=
NM_001382394.1:c.1547G= NP_001369323.1:p.Ser516=
NM_001382395.1:c.1568G= NP_001369324.1:p.Ser523=
NM_005633.4:c.1568G= MANE Select NP_005624.2:p.Ser523=
Search 100 bp 5'
Search 100 bp 3'