Canonical Allele Identifier: CA346373155
Gene: SOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054728A>T , CM000664.2:g.39054728A>T GRCh38
NC_000002.11:g.39281869A>T , CM000664.1:g.39281869A>T GRCh37
NC_000002.10:g.39135373A>T NCBI36
NG_007530.1:g.70736T>A , LRG_754:g.70736T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.633T>A
ENST00000685782.1:n.1444T>A
ENST00000688189.1:n.371T>A
ENST00000689668.1:n.613T>A
ENST00000690679.1:c.706T>A
ENST00000690876.1:c.606T>A ENSP00000508955.1:p.Tyr202Ter
ENST00000691229.1:c.606T>A ENSP00000510437.1:p.Tyr202Ter
ENST00000692089.1:c.606T>A ENSP00000508626.1:p.Tyr202Ter
ENST00000402219.8:c.606T>A MANE Select ENSP00000384675.2:p.Tyr202Ter
ENST00000395038.6:c.606T>A ENSP00000378479.2:p.Tyr202Ter
ENST00000402219.6:c.606T>A ENSP00000384675.2:p.Tyr202Ter
ENST00000426016.5:c.606T>A ENSP00000387784.1:p.Tyr202Ter
NM_005633.3:c.606T>A , LRG_754t1:c.606T>A NP_005624.2:p.Tyr202Ter
XM_005264515.3:c.606T>A XP_005264572.1:p.Tyr202Ter
XM_011533060.1:c.699T>A XP_011531362.1:p.Tyr233Ter
XM_011533061.1:c.699T>A XP_011531363.1:p.Tyr233Ter
XM_011533062.1:c.585T>A XP_011531364.1:p.Tyr195Ter
XM_011533063.1:c.582T>A XP_011531365.1:p.Tyr194Ter
XM_011533064.1:c.435T>A XP_011531366.1:p.Tyr145Ter
XM_011533065.1:c.699T>A XP_011531367.1:p.Tyr233Ter
XM_005264515.4:c.606T>A XP_005264572.1:p.Tyr202Ter
XM_011533062.2:c.585T>A XP_011531364.1:p.Tyr195Ter
XM_011533064.2:c.435T>A XP_011531366.1:p.Tyr145Ter
NM_001382394.1:c.585T>A NP_001369323.1:p.Tyr195Ter
NM_001382395.1:c.606T>A NP_001369324.1:p.Tyr202Ter
NM_005633.4:c.606T>A MANE Select NP_005624.2:p.Tyr202Ter