Canonical Allele Identifier: CA1246123928

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38996981A= , CM000664.2:g.38996981A=	GRCh38
NC_000002.11:g.39224122A= , CM000664.1:g.39224122A=	GRCh37
NC_000002.10:g.39077626A=	NCBI36
NG_007530.1:g.128483T= , LRG_754:g.128483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.1789T=	ENSP00000509424.1:p.Tyr597=
ENST00000689668.1:n.3029T=
ENST00000690876.1:c.*328T=	ENSP00000508955.1:n.*328T=
ENST00000691229.1:c.2791T=	ENSP00000510437.1:p.Tyr931=
ENST00000692089.1:c.2911T=	ENSP00000508626.1:p.Tyr971=
ENST00000692227.1:c.718T=	ENSP00000509138.1:p.Tyr240=
ENST00000692620.1:c.*609T=	ENSP00000509311.1:n.*609T=
ENST00000402219.8:c.3022T= MANE Select	ENSP00000384675.2:p.Tyr1008=
ENST00000395038.6:c.3022T=	ENSP00000378479.2:p.Tyr1008=
ENST00000402219.6:c.3022T=	ENSP00000384675.2:p.Tyr1008=
ENST00000426016.5:c.3022T=	ENSP00000387784.1:p.Tyr1008=
NM_005633.3:c.3022T= , LRG_754t1:c.3022T=	NP_005624.2:p.Tyr1008=
XM_005264515.3:c.3022T=	XP_005264572.1:p.Tyr1008=
XM_011533060.1:c.3115T=	XP_011531362.1:p.Tyr1039=
XM_011533061.1:c.3115T=	XP_011531363.1:p.Tyr1039=
XM_011533062.1:c.3001T=	XP_011531364.1:p.Tyr1001=
XM_011533063.1:c.2998T=	XP_011531365.1:p.Tyr1000=
XM_011533064.1:c.2851T=	XP_011531366.1:p.Tyr951=
XM_011533065.1:c.3115T=	XP_011531367.1:p.Tyr1039=
XM_011533066.1:c.1957T=	XP_011531368.1:p.Tyr653=
XM_005264515.4:c.3022T=	XP_005264572.1:p.Tyr1008=
XM_011533062.2:c.3001T=	XP_011531364.1:p.Tyr1001=
XM_011533064.2:c.2851T=	XP_011531366.1:p.Tyr951=
NM_001382394.1:c.3001T=	NP_001369323.1:p.Tyr1001=
NM_001382395.1:c.3022T=	NP_001369324.1:p.Tyr1008=
NM_005633.4:c.3022T= MANE Select	NP_005624.2:p.Tyr1008=