Canonical Allele Identifier: CA1246153927

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054715C= , CM000664.2:g.39054715C=	GRCh38
NC_000002.11:g.39281856C= , CM000664.1:g.39281856C=	GRCh37
NC_000002.10:g.39135360C=	NCBI36
NG_007530.1:g.70749G= , LRG_754:g.70749G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.646G=
ENST00000685782.1:n.1457G=
ENST00000688189.1:n.384G=
ENST00000689668.1:n.626G=
ENST00000690679.1:c.719G=
ENST00000690876.1:c.619G=	ENSP00000508955.1:p.Ala207=
ENST00000691229.1:c.619G=	ENSP00000510437.1:p.Ala207=
ENST00000692089.1:c.619G=	ENSP00000508626.1:p.Ala207=
ENST00000402219.8:c.619G= MANE Select	ENSP00000384675.2:p.Ala207=
ENST00000395038.6:c.619G=	ENSP00000378479.2:p.Ala207=
ENST00000402219.6:c.619G=	ENSP00000384675.2:p.Ala207=
ENST00000426016.5:c.619G=	ENSP00000387784.1:p.Ala207=
NM_005633.3:c.619G= , LRG_754t1:c.619G=	NP_005624.2:p.Ala207=
XM_005264515.3:c.619G=	XP_005264572.1:p.Ala207=
XM_011533060.1:c.712G=	XP_011531362.1:p.Ala238=
XM_011533061.1:c.712G=	XP_011531363.1:p.Ala238=
XM_011533062.1:c.598G=	XP_011531364.1:p.Ala200=
XM_011533063.1:c.595G=	XP_011531365.1:p.Ala199=
XM_011533064.1:c.448G=	XP_011531366.1:p.Ala150=
XM_011533065.1:c.712G=	XP_011531367.1:p.Ala238=
XM_005264515.4:c.619G=	XP_005264572.1:p.Ala207=
XM_011533062.2:c.598G=	XP_011531364.1:p.Ala200=
XM_011533064.2:c.448G=	XP_011531366.1:p.Ala150=
NM_001382394.1:c.598G=	NP_001369323.1:p.Ala200=
NM_001382395.1:c.619G=	NP_001369324.1:p.Ala207=
NM_005633.4:c.619G= MANE Select	NP_005624.2:p.Ala207=