Canonical Allele Identifier: CA1246139517

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022782G= , CM000664.2:g.39022782G=	GRCh38
NC_000002.11:g.39249923G= , CM000664.1:g.39249923G=	GRCh37
NC_000002.10:g.39103427G=	NCBI36
NG_007530.1:g.102682C= , LRG_754:g.102682C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000472480.2:n.1526C=
ENST00000685279.1:c.413C=	ENSP00000509424.1:p.Thr138=
ENST00000688043.1:n.1867C=
ENST00000689668.1:n.1653C=
ENST00000690876.1:c.1535C=	ENSP00000508955.1:p.Thr512=
ENST00000691229.1:c.1535C=	ENSP00000510437.1:p.Thr512=
ENST00000692089.1:c.1535C=	ENSP00000508626.1:p.Thr512=
ENST00000692620.1:c.413C=	ENSP00000509311.1:p.Thr138=
ENST00000402219.8:c.1646C= MANE Select	ENSP00000384675.2:p.Thr549=
ENST00000395038.6:c.1646C=	ENSP00000378479.2:p.Thr549=
ENST00000402219.6:c.1646C=	ENSP00000384675.2:p.Thr549=
ENST00000426016.5:c.1646C=	ENSP00000387784.1:p.Thr549=
NM_005633.3:c.1646C= , LRG_754t1:c.1646C=	NP_005624.2:p.Thr549=
XM_005264515.3:c.1646C=	XP_005264572.1:p.Thr549=
XM_011533060.1:c.1739C=	XP_011531362.1:p.Thr580=
XM_011533061.1:c.1739C=	XP_011531363.1:p.Thr580=
XM_011533062.1:c.1625C=	XP_011531364.1:p.Thr542=
XM_011533063.1:c.1622C=	XP_011531365.1:p.Thr541=
XM_011533064.1:c.1475C=	XP_011531366.1:p.Thr492=
XM_011533065.1:c.1739C=	XP_011531367.1:p.Thr580=
XM_011533066.1:c.581C=	XP_011531368.1:p.Thr194=
XM_005264515.4:c.1646C=	XP_005264572.1:p.Thr549=
XM_011533062.2:c.1625C=	XP_011531364.1:p.Thr542=
XM_011533064.2:c.1475C=	XP_011531366.1:p.Thr492=
NM_001382394.1:c.1625C=	NP_001369323.1:p.Thr542=
NM_001382395.1:c.1646C=	NP_001369324.1:p.Thr549=
NM_005633.4:c.1646C= MANE Select	NP_005624.2:p.Thr549=