Canonical Allele Identifier: CA1246131343

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39012236T= , CM000664.2:g.39012236T=	GRCh38
NC_000002.11:g.39239377T= , CM000664.1:g.39239377T=	GRCh37
NC_000002.10:g.39092881T=	NCBI36
NG_007530.1:g.113228A= , LRG_754:g.113228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.1047A=	ENSP00000509424.1:p.Thr349=
ENST00000688043.1:n.3612A=
ENST00000689668.1:n.2287A=
ENST00000690514.1:n.369A=
ENST00000690876.1:c.2169A=	ENSP00000508955.1:p.Thr723=
ENST00000691229.1:c.2169A=	ENSP00000510437.1:p.Thr723=
ENST00000692089.1:c.2169A=	ENSP00000508626.1:p.Thr723=
ENST00000692620.1:c.934+1224A=	ENSP00000509311.1:n.934+1224A=
ENST00000402219.8:c.2280A= MANE Select	ENSP00000384675.2:p.Thr760=
ENST00000395038.6:c.2280A=	ENSP00000378479.2:p.Thr760=
ENST00000402219.6:c.2280A=	ENSP00000384675.2:p.Thr760=
ENST00000426016.5:c.2280A=	ENSP00000387784.1:p.Thr760=
NM_005633.3:c.2280A= , LRG_754t1:c.2280A=	NP_005624.2:p.Thr760=
XM_005264515.3:c.2280A=	XP_005264572.1:p.Thr760=
XM_011533060.1:c.2373A=	XP_011531362.1:p.Thr791=
XM_011533061.1:c.2373A=	XP_011531363.1:p.Thr791=
XM_011533062.1:c.2259A=	XP_011531364.1:p.Thr753=
XM_011533063.1:c.2256A=	XP_011531365.1:p.Thr752=
XM_011533064.1:c.2109A=	XP_011531366.1:p.Thr703=
XM_011533065.1:c.2373A=	XP_011531367.1:p.Thr791=
XM_011533066.1:c.1215A=	XP_011531368.1:p.Thr405=
XM_005264515.4:c.2280A=	XP_005264572.1:p.Thr760=
XM_011533062.2:c.2259A=	XP_011531364.1:p.Thr753=
XM_011533064.2:c.2109A=	XP_011531366.1:p.Thr703=
NM_001382394.1:c.2259A=	NP_001369323.1:p.Thr753=
NM_001382395.1:c.2280A=	NP_001369324.1:p.Thr760=
NM_005633.4:c.2280A= MANE Select	NP_005624.2:p.Thr760=