Canonical Allele Identifier: CA1246131376

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39012319T= , CM000664.2:g.39012319T=	GRCh38
NC_000002.11:g.39239460T= , CM000664.1:g.39239460T=	GRCh37
NC_000002.10:g.39092964T=	NCBI36
NG_007530.1:g.113145A= , LRG_754:g.113145A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.964A=	ENSP00000509424.1:p.Ile322=
ENST00000688043.1:n.3529A=
ENST00000689668.1:n.2204A=
ENST00000690514.1:n.286A=
ENST00000690876.1:c.2086A=	ENSP00000508955.1:p.Ile696=
ENST00000691229.1:c.2086A=	ENSP00000510437.1:p.Ile696=
ENST00000692089.1:c.2086A=	ENSP00000508626.1:p.Ile696=
ENST00000692620.1:c.934+1141A=	ENSP00000509311.1:n.934+1141A=
ENST00000402219.8:c.2197A= MANE Select	ENSP00000384675.2:p.Ile733=
ENST00000395038.6:c.2197A=	ENSP00000378479.2:p.Ile733=
ENST00000402219.6:c.2197A=	ENSP00000384675.2:p.Ile733=
ENST00000426016.5:c.2197A=	ENSP00000387784.1:p.Ile733=
NM_005633.3:c.2197A= , LRG_754t1:c.2197A=	NP_005624.2:p.Ile733=
XM_005264515.3:c.2197A=	XP_005264572.1:p.Ile733=
XM_011533060.1:c.2290A=	XP_011531362.1:p.Ile764=
XM_011533061.1:c.2290A=	XP_011531363.1:p.Ile764=
XM_011533062.1:c.2176A=	XP_011531364.1:p.Ile726=
XM_011533063.1:c.2173A=	XP_011531365.1:p.Ile725=
XM_011533064.1:c.2026A=	XP_011531366.1:p.Ile676=
XM_011533065.1:c.2290A=	XP_011531367.1:p.Ile764=
XM_011533066.1:c.1132A=	XP_011531368.1:p.Ile378=
XM_005264515.4:c.2197A=	XP_005264572.1:p.Ile733=
XM_011533062.2:c.2176A=	XP_011531364.1:p.Ile726=
XM_011533064.2:c.2026A=	XP_011531366.1:p.Ile676=
NM_001382394.1:c.2176A=	NP_001369323.1:p.Ile726=
NM_001382395.1:c.2197A=	NP_001369324.1:p.Ile733=
NM_005633.4:c.2197A= MANE Select	NP_005624.2:p.Ile733=