Canonical Allele Identifier: CA1246140177

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023198C= , CM000664.2:g.39023198C=	GRCh38
NC_000002.11:g.39250339C= , CM000664.1:g.39250339C=	GRCh37
NC_000002.10:g.39103843C=	NCBI36
NG_007530.1:g.102266G= , LRG_754:g.102266G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1110G=
ENST00000685279.1:c.-4G=	ENSP00000509424.1:n.-4G=
ENST00000688043.1:n.1451G=
ENST00000689668.1:n.1237G=
ENST00000690679.1:c.1417G=
ENST00000690876.1:c.1119G=	ENSP00000508955.1:p.Gln373=
ENST00000691229.1:c.1119G=	ENSP00000510437.1:p.Gln373=
ENST00000692089.1:c.1119G=	ENSP00000508626.1:p.Gln373=
ENST00000692620.1:c.-4G=	ENSP00000509311.1:n.-4G=
ENST00000402219.8:c.1230G= MANE Select	ENSP00000384675.2:p.Gln410=
ENST00000395038.6:c.1230G=	ENSP00000378479.2:p.Gln410=
ENST00000402219.6:c.1230G=	ENSP00000384675.2:p.Gln410=
ENST00000426016.5:c.1230G=	ENSP00000387784.1:p.Gln410=
ENST00000472480.1:n.74G=
NM_005633.3:c.1230G= , LRG_754t1:c.1230G=	NP_005624.2:p.Gln410=
XM_005264515.3:c.1230G=	XP_005264572.1:p.Gln410=
XM_011533060.1:c.1323G=	XP_011531362.1:p.Gln441=
XM_011533061.1:c.1323G=	XP_011531363.1:p.Gln441=
XM_011533062.1:c.1209G=	XP_011531364.1:p.Gln403=
XM_011533063.1:c.1206G=	XP_011531365.1:p.Gln402=
XM_011533064.1:c.1059G=	XP_011531366.1:p.Gln353=
XM_011533065.1:c.1323G=	XP_011531367.1:p.Gln441=
XM_011533066.1:c.165G=	XP_011531368.1:p.Gln55=
XM_005264515.4:c.1230G=	XP_005264572.1:p.Gln410=
XM_011533062.2:c.1209G=	XP_011531364.1:p.Gln403=
XM_011533064.2:c.1059G=	XP_011531366.1:p.Gln353=
NM_001382394.1:c.1209G=	NP_001369323.1:p.Gln403=
NM_001382395.1:c.1230G=	NP_001369324.1:p.Gln410=
NM_005633.4:c.1230G= MANE Select	NP_005624.2:p.Gln410=