Canonical Allele Identifier: CA1246139855

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022970T= , CM000664.2:g.39022970T=	GRCh38
NC_000002.11:g.39250111T= , CM000664.1:g.39250111T=	GRCh37
NC_000002.10:g.39103615T=	NCBI36
NG_007530.1:g.102494A= , LRG_754:g.102494A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1338A=
ENST00000685279.1:c.225A=	ENSP00000509424.1:p.Ala75=
ENST00000688043.1:n.1679A=
ENST00000689668.1:n.1465A=
ENST00000690876.1:c.1347A=	ENSP00000508955.1:p.Ala449=
ENST00000691229.1:c.1347A=	ENSP00000510437.1:p.Ala449=
ENST00000692089.1:c.1347A=	ENSP00000508626.1:p.Ala449=
ENST00000692620.1:c.225A=	ENSP00000509311.1:p.Ala75=
ENST00000402219.8:c.1458A= MANE Select	ENSP00000384675.2:p.Ala486=
ENST00000395038.6:c.1458A=	ENSP00000378479.2:p.Ala486=
ENST00000402219.6:c.1458A=	ENSP00000384675.2:p.Ala486=
ENST00000426016.5:c.1458A=	ENSP00000387784.1:p.Ala486=
ENST00000472480.1:n.302A=
NM_005633.3:c.1458A= , LRG_754t1:c.1458A=	NP_005624.2:p.Ala486=
XM_005264515.3:c.1458A=	XP_005264572.1:p.Ala486=
XM_011533060.1:c.1551A=	XP_011531362.1:p.Ala517=
XM_011533061.1:c.1551A=	XP_011531363.1:p.Ala517=
XM_011533062.1:c.1437A=	XP_011531364.1:p.Ala479=
XM_011533063.1:c.1434A=	XP_011531365.1:p.Ala478=
XM_011533064.1:c.1287A=	XP_011531366.1:p.Ala429=
XM_011533065.1:c.1551A=	XP_011531367.1:p.Ala517=
XM_011533066.1:c.393A=	XP_011531368.1:p.Ala131=
XM_005264515.4:c.1458A=	XP_005264572.1:p.Ala486=
XM_011533062.2:c.1437A=	XP_011531364.1:p.Ala479=
XM_011533064.2:c.1287A=	XP_011531366.1:p.Ala429=
NM_001382394.1:c.1437A=	NP_001369323.1:p.Ala479=
NM_001382395.1:c.1458A=	NP_001369324.1:p.Ala486=
NM_005633.4:c.1458A= MANE Select	NP_005624.2:p.Ala486=