Canonical Allele Identifier: CA1246139235
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022633G= , CM000664.2:g.39022633G= GRCh38
NC_000002.11:g.39249774G= , CM000664.1:g.39249774G= GRCh37
NC_000002.10:g.39103278G= NCBI36
NG_007530.1:g.102831C= , LRG_754:g.102831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1675C=
ENST00000685279.1:c.562C= ENSP00000509424.1:p.Pro188=
ENST00000688043.1:n.2016C=
ENST00000689668.1:n.1802C=
ENST00000690876.1:c.1684C= ENSP00000508955.1:p.Pro562=
ENST00000691229.1:c.1684C= ENSP00000510437.1:p.Pro562=
ENST00000692089.1:c.1684C= ENSP00000508626.1:p.Pro562=
ENST00000692620.1:c.562C= ENSP00000509311.1:p.Pro188=
ENST00000402219.8:c.1795C= MANE Select ENSP00000384675.2:p.Pro599=
ENST00000395038.6:c.1795C= ENSP00000378479.2:p.Pro599=
ENST00000402219.6:c.1795C= ENSP00000384675.2:p.Pro599=
ENST00000426016.5:c.1795C= ENSP00000387784.1:p.Pro599=
NM_005633.3:c.1795C= , LRG_754t1:c.1795C= NP_005624.2:p.Pro599=
XM_005264515.3:c.1795C= XP_005264572.1:p.Pro599=
XM_011533060.1:c.1888C= XP_011531362.1:p.Pro630=
XM_011533061.1:c.1888C= XP_011531363.1:p.Pro630=
XM_011533062.1:c.1774C= XP_011531364.1:p.Pro592=
XM_011533063.1:c.1771C= XP_011531365.1:p.Pro591=
XM_011533064.1:c.1624C= XP_011531366.1:p.Pro542=
XM_011533065.1:c.1888C= XP_011531367.1:p.Pro630=
XM_011533066.1:c.730C= XP_011531368.1:p.Pro244=
XM_005264515.4:c.1795C= XP_005264572.1:p.Pro599=
XM_011533062.2:c.1774C= XP_011531364.1:p.Pro592=
XM_011533064.2:c.1624C= XP_011531366.1:p.Pro542=
NM_001382394.1:c.1774C= NP_001369323.1:p.Pro592=
NM_001382395.1:c.1795C= NP_001369324.1:p.Pro599=
NM_005633.4:c.1795C= MANE Select NP_005624.2:p.Pro599=
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