Canonical Allele Identifier: CA1246140241

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023352_39023357delinsATAGAT , CM000664.2:g.39023352_39023357delinsATAGAT	GRCh38
NC_000002.11:g.39250493_39250498delinsATAGAT , CM000664.1:g.39250493_39250498delinsATAGAT	GRCh37
NC_000002.10:g.39103997_39104002delinsATAGAT	NCBI36
NG_007530.1:g.102107_102112delinsATCTAT , LRG_754:g.102107_102112delinsATCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083-132_1083-127delinsATCTAT
ENST00000685279.1:c.-31-132_-31-127delinsATCTAT	ENSP00000509424.1:n.-31-132_-31-127delinsATCTAT
ENST00000688043.1:n.1424-132_1424-127delinsATCTAT
ENST00000689668.1:n.1210-132_1210-127delinsATCTAT
ENST00000690679.1:c.1390-132_1390-127delinsATCTAT
ENST00000690876.1:c.1092-132_1092-127delinsATCTAT	ENSP00000508955.1:n.1092-132_1092-127delinsATCTAT
ENST00000691229.1:c.1092-132_1092-127delinsATCTAT	ENSP00000510437.1:n.1092-132_1092-127delinsATCTAT
ENST00000692089.1:c.1092-132_1092-127delinsATCTAT	ENSP00000508626.1:n.1092-132_1092-127delinsATCTAT
ENST00000692620.1:c.-31-132_-31-127delinsATCTAT	ENSP00000509311.1:n.-31-132_-31-127delinsATCTAT
ENST00000402219.8:c.1203-132_1203-127delinsATCTAT MANE Select	ENSP00000384675.2:n.1203-132_1203-127delinsATCTAT
ENST00000395038.6:c.1203-132_1203-127delinsATCTAT	ENSP00000378479.2:n.1203-132_1203-127delinsATCTAT
ENST00000402219.6:c.1203-132_1203-127delinsATCTAT	ENSP00000384675.2:n.1203-132_1203-127delinsATCTAT
ENST00000426016.5:c.1203-132_1203-127delinsATCTAT	ENSP00000387784.1:n.1203-132_1203-127delinsATCTAT
ENST00000472480.1:n.47-132_47-127delinsATCTAT
NM_005633.3:c.1203-132_1203-127delinsATCTAT , LRG_754t1:c.1203-132_1203-127delinsATCTAT	NP_005624.2:n.1203-132_1203-127delinsATCTAT
XM_005264515.3:c.1203-132_1203-127delinsATCTAT	XP_005264572.1:n.1203-132_1203-127delinsATCTAT
XM_011533060.1:c.1296-132_1296-127delinsATCTAT	XP_011531362.1:n.1296-132_1296-127delinsATCTAT
XM_011533061.1:c.1296-132_1296-127delinsATCTAT	XP_011531363.1:n.1296-132_1296-127delinsATCTAT
XM_011533062.1:c.1182-132_1182-127delinsATCTAT	XP_011531364.1:n.1182-132_1182-127delinsATCTAT
XM_011533063.1:c.1179-132_1179-127delinsATCTAT	XP_011531365.1:n.1179-132_1179-127delinsATCTAT
XM_011533064.1:c.1032-132_1032-127delinsATCTAT	XP_011531366.1:n.1032-132_1032-127delinsATCTAT
XM_011533065.1:c.1296-132_1296-127delinsATCTAT	XP_011531367.1:n.1296-132_1296-127delinsATCTAT
XM_011533066.1:c.138-132_138-127delinsATCTAT	XP_011531368.1:n.138-132_138-127delinsATCTAT
XM_005264515.4:c.1203-132_1203-127delinsATCTAT	XP_005264572.1:n.1203-132_1203-127delinsATCTAT
XM_011533062.2:c.1182-132_1182-127delinsATCTAT	XP_011531364.1:n.1182-132_1182-127delinsATCTAT
XM_011533064.2:c.1032-132_1032-127delinsATCTAT	XP_011531366.1:n.1032-132_1032-127delinsATCTAT
NM_001382394.1:c.1182-132_1182-127delinsATCTAT	NP_001369323.1:n.1182-132_1182-127delinsATCTAT
NM_001382395.1:c.1203-132_1203-127delinsATCTAT	NP_001369324.1:n.1203-132_1203-127delinsATCTAT
NM_005633.4:c.1203-132_1203-127delinsATCTAT MANE Select	NP_005624.2:n.1203-132_1203-127delinsATCTAT