Canonical Allele Identifier: CA3090197943

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39013535C= , CM000664.2:g.39013535C=	GRCh38
NC_000002.11:g.39240676C= , CM000664.1:g.39240676C=	GRCh37
NC_000002.10:g.39094180C=	NCBI36
NG_007530.1:g.111929G= , LRG_754:g.111929G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005633.4:c.2092G= MANE Select	NP_005624.2:p.Glu698=
ENST00000402219.8:c.2092G= MANE Select	ENSP00000384675.2:p.Glu698=
NM_001382394.1:c.2071G=	NP_001369323.1:p.Glu691=
NM_001382395.1:c.2092G=	NP_001369324.1:p.Glu698=
NM_005633.3:c.2092G= , LRG_754t1:c.2092G=	NP_005624.2:p.Glu698=
ENST00000395038.6:c.2092G=	ENSP00000378479.2:p.Glu698=
ENST00000402219.6:c.2092G=	ENSP00000384675.2:p.Glu698=
ENST00000426016.5:c.2092G=	ENSP00000387784.1:p.Glu698=
ENST00000685279.1:c.859G=	ENSP00000509424.1:p.Glu287=
ENST00000688043.1:n.2313G=
ENST00000689668.1:n.2099G=
ENST00000690514.1:n.181G=
ENST00000690876.1:c.1981G=	ENSP00000508955.1:p.Glu661=
ENST00000691229.1:c.1981G=	ENSP00000510437.1:p.Glu661=
ENST00000692089.1:c.1981G=	ENSP00000508626.1:p.Glu661=
ENST00000692620.1:c.859G=	ENSP00000509311.1:p.Glu287=
XM_005264515.3:c.2092G=	XP_005264572.1:p.Glu698=
XM_005264515.4:c.2092G=	XP_005264572.1:p.Glu698=
XM_011533060.1:c.2185G=	XP_011531362.1:p.Glu729=
XM_011533061.1:c.2185G=	XP_011531363.1:p.Glu729=
XM_011533062.1:c.2071G=	XP_011531364.1:p.Glu691=
XM_011533062.2:c.2071G=	XP_011531364.1:p.Glu691=
XM_011533063.1:c.2068G=	XP_011531365.1:p.Glu690=
XM_011533064.1:c.1921G=	XP_011531366.1:p.Glu641=
XM_011533064.2:c.1921G=	XP_011531366.1:p.Glu641=
XM_011533065.1:c.2185G=	XP_011531367.1:p.Glu729=
XM_011533066.1:c.1027G=	XP_011531368.1:p.Glu343=