Canonical Allele Identifier: CA45671346
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38983250T>C , CM000664.2:g.38983250T>C GRCh38
NC_000002.11:g.39210391T>C , CM000664.1:g.39210391T>C GRCh37
NC_000002.10:g.39063895T>C NCBI36
NG_007530.1:g.142214A>G , LRG_754:g.142214A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000685279.1:c.*2574A>G ENSP00000509424.1:n.*2574A>G
ENST00000692089.1:c.3399+4223A>G ENSP00000508626.1:n.3399+4223A>G
ENST00000402219.8:c.*2574A>G MANE Select ENSP00000384675.2:n.*2574A>G
ENST00000402219.6:c.*2574A>G ENSP00000384675.2:n.*2574A>G
ENST00000426016.5:c.*2574A>G ENSP00000387784.1:n.*2574A>G
NM_005633.3:c.*2574A>G , LRG_754t1:c.*2574A>G NP_005624.2:n.*2574A>G
XM_005264515.3:c.*2574A>G XP_005264572.1:n.*2574A>G
XM_011533060.1:c.*2574A>G XP_011531362.1:n.*2574A>G
XM_011533061.1:c.*2574A>G XP_011531363.1:n.*2574A>G
XM_011533062.1:c.*2574A>G XP_011531364.1:n.*2574A>G
XM_011533063.1:c.*2574A>G XP_011531365.1:n.*2574A>G
XM_011533064.1:c.*2574A>G XP_011531366.1:n.*2574A>G
XM_011533065.1:c.*2060A>G XP_011531367.1:n.*2060A>G
XM_011533066.1:c.*2574A>G XP_011531368.1:n.*2574A>G
XM_005264515.4:c.*2574A>G XP_005264572.1:n.*2574A>G
NM_001382394.1:c.*2574A>G NP_001369323.1:n.*2574A>G
NM_001382395.1:c.*2574A>G NP_001369324.1:n.*2574A>G
NM_005633.4:c.*2574A>G MANE Select NP_005624.2:n.*2574A>G