Canonical Allele Identifier: CA1624825
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448945
dbSNP Id: rs144757941
gnomAD v2: 2-39285879-T-C
gnomAD v3: 2-39058738-T-C
gnomAD v4: 2-39058738-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39058738T>C , CM000664.2:g.39058738T>C GRCh38
NC_000002.11:g.39285879T>C , CM000664.1:g.39285879T>C GRCh37
NC_000002.10:g.39139383T>C NCBI36
NG_007530.1:g.66726A>G , LRG_754:g.66726A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.307A>G
ENST00000685782.1:n.1118A>G
ENST00000688189.1:n.45A>G
ENST00000689668.1:n.287A>G
ENST00000690679.1:c.380A>G
ENST00000690876.1:c.280A>G ENSP00000508955.1:p.Ile94Val
ENST00000691229.1:c.280A>G ENSP00000510437.1:p.Ile94Val
ENST00000692089.1:c.280A>G ENSP00000508626.1:p.Ile94Val
ENST00000402219.8:c.280A>G MANE Select ENSP00000384675.2:p.Ile94Val
ENST00000395038.6:c.280A>G ENSP00000378479.2:p.Ile94Val
ENST00000402219.6:c.280A>G ENSP00000384675.2:p.Ile94Val
ENST00000426016.5:c.280A>G ENSP00000387784.1:p.Ile94Val
ENST00000451331.1:c.109A>G ENSP00000393899.1:p.Ile37Val
NM_005633.3:c.280A>G , LRG_754t1:c.280A>G NP_005624.2:p.Ile94Val
XM_005264515.3:c.280A>G XP_005264572.1:p.Ile94Val
XM_011533060.1:c.373A>G XP_011531362.1:p.Ile125Val
XM_011533061.1:c.373A>G XP_011531363.1:p.Ile125Val
XM_011533062.1:c.259A>G XP_011531364.1:p.Ile87Val
XM_011533063.1:c.256A>G XP_011531365.1:p.Ile86Val
XM_011533064.1:c.109A>G XP_011531366.1:p.Ile37Val
XM_011533065.1:c.373A>G XP_011531367.1:p.Ile125Val
XM_005264515.4:c.280A>G XP_005264572.1:p.Ile94Val
XM_011533062.2:c.259A>G XP_011531364.1:p.Ile87Val
XM_011533064.2:c.109A>G XP_011531366.1:p.Ile37Val
NM_001382394.1:c.259A>G NP_001369323.1:p.Ile87Val
NM_001382395.1:c.280A>G NP_001369324.1:p.Ile94Val
NM_005633.4:c.280A>G MANE Select NP_005624.2:p.Ile94Val