Canonical Allele Identifier: CA346365971
Gene: SOS1 HGNC NCBI

Linked Data

gnomAD v4: 2-39022903-C-T
COSMIC: COSM1020876
MyVariant Identifiers: chr2:g.39250044C>T (hg19) chr2:g.39022903C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022903C>T , CM000664.2:g.39022903C>T GRCh38
NC_000002.11:g.39250044C>T , CM000664.1:g.39250044C>T GRCh37
NC_000002.10:g.39103548C>T NCBI36
NG_007530.1:g.102561G>A , LRG_754:g.102561G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1405G>A
ENST00000685279.1:c.292G>A ENSP00000509424.1:p.Glu98Lys
ENST00000688043.1:n.1746G>A
ENST00000689668.1:n.1532G>A
ENST00000690876.1:c.1414G>A ENSP00000508955.1:p.Glu472Lys
ENST00000691229.1:c.1414G>A ENSP00000510437.1:p.Glu472Lys
ENST00000692089.1:c.1414G>A ENSP00000508626.1:p.Glu472Lys
ENST00000692620.1:c.292G>A ENSP00000509311.1:p.Glu98Lys
ENST00000402219.8:c.1525G>A MANE Select ENSP00000384675.2:p.Glu509Lys
ENST00000395038.6:c.1525G>A ENSP00000378479.2:p.Glu509Lys
ENST00000402219.6:c.1525G>A ENSP00000384675.2:p.Glu509Lys
ENST00000426016.5:c.1525G>A ENSP00000387784.1:p.Glu509Lys
ENST00000472480.1:n.369G>A
NM_005633.3:c.1525G>A , LRG_754t1:c.1525G>A NP_005624.2:p.Glu509Lys
XM_005264515.3:c.1525G>A XP_005264572.1:p.Glu509Lys
XM_011533060.1:c.1618G>A XP_011531362.1:p.Glu540Lys
XM_011533061.1:c.1618G>A XP_011531363.1:p.Glu540Lys
XM_011533062.1:c.1504G>A XP_011531364.1:p.Glu502Lys
XM_011533063.1:c.1501G>A XP_011531365.1:p.Glu501Lys
XM_011533064.1:c.1354G>A XP_011531366.1:p.Glu452Lys
XM_011533065.1:c.1618G>A XP_011531367.1:p.Glu540Lys
XM_011533066.1:c.460G>A XP_011531368.1:p.Glu154Lys
XM_005264515.4:c.1525G>A XP_005264572.1:p.Glu509Lys
XM_011533062.2:c.1504G>A XP_011531364.1:p.Glu502Lys
XM_011533064.2:c.1354G>A XP_011531366.1:p.Glu452Lys
NM_001382394.1:c.1504G>A NP_001369323.1:p.Glu502Lys
NM_001382395.1:c.1525G>A NP_001369324.1:p.Glu509Lys
NM_005633.4:c.1525G>A MANE Select NP_005624.2:p.Glu509Lys
Search 100 bp 5'
Search 100 bp 3'