Canonical Allele Identifier: CA1246140145

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023134_39023135delinsAA , CM000664.2:g.39023134_39023135delinsAA	GRCh38
NC_000002.11:g.39250275_39250276delinsAA , CM000664.1:g.39250275_39250276delinsAA	GRCh37
NC_000002.10:g.39103779_39103780delinsAA	NCBI36
NG_007530.1:g.102329_102330delinsTT , LRG_754:g.102329_102330delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1173_1174delinsTT
ENST00000685279.1:c.60_61delinsTT	ENSP00000509424.1:p.Gly20=
ENST00000688043.1:n.1514_1515delinsTT
ENST00000689668.1:n.1300_1301delinsTT
ENST00000690876.1:c.1182_1183delinsTT	ENSP00000508955.1:p.Gly394=
ENST00000691229.1:c.1182_1183delinsTT	ENSP00000510437.1:p.Gly394=
ENST00000692089.1:c.1182_1183delinsTT	ENSP00000508626.1:p.Gly394=
ENST00000692620.1:c.60_61delinsTT	ENSP00000509311.1:p.Gly20=
ENST00000402219.8:c.1293_1294delinsTT MANE Select	ENSP00000384675.2:p.Gly431=
ENST00000395038.6:c.1293_1294delinsTT	ENSP00000378479.2:p.Gly431=
ENST00000402219.6:c.1293_1294delinsTT	ENSP00000384675.2:p.Gly431=
ENST00000426016.5:c.1293_1294delinsTT	ENSP00000387784.1:p.Gly431=
ENST00000472480.1:n.137_138delinsTT
NM_005633.3:c.1293_1294delinsTT , LRG_754t1:c.1293_1294delinsTT	NP_005624.2:p.Gly431=
XM_005264515.3:c.1293_1294delinsTT	XP_005264572.1:p.Gly431=
XM_011533060.1:c.1386_1387delinsTT	XP_011531362.1:p.Gly462=
XM_011533061.1:c.1386_1387delinsTT	XP_011531363.1:p.Gly462=
XM_011533062.1:c.1272_1273delinsTT	XP_011531364.1:p.Gly424=
XM_011533063.1:c.1269_1270delinsTT	XP_011531365.1:p.Gly423=
XM_011533064.1:c.1122_1123delinsTT	XP_011531366.1:p.Gly374=
XM_011533065.1:c.1386_1387delinsTT	XP_011531367.1:p.Gly462=
XM_011533066.1:c.228_229delinsTT	XP_011531368.1:p.Gly76=
XM_005264515.4:c.1293_1294delinsTT	XP_005264572.1:p.Gly431=
XM_011533062.2:c.1272_1273delinsTT	XP_011531364.1:p.Gly424=
XM_011533064.2:c.1122_1123delinsTT	XP_011531366.1:p.Gly374=
NM_001382394.1:c.1272_1273delinsTT	NP_001369323.1:p.Gly424=
NM_001382395.1:c.1293_1294delinsTT	NP_001369324.1:p.Gly431=
NM_005633.4:c.1293_1294delinsTT MANE Select	NP_005624.2:p.Gly431=