Canonical Allele Identifier: CA1246140201

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023258_39023259delinsAG , CM000664.2:g.39023258_39023259delinsAG	GRCh38
NC_000002.11:g.39250399_39250400delinsAG , CM000664.1:g.39250399_39250400delinsAG	GRCh37
NC_000002.10:g.39103903_39103904delinsAG	NCBI36
NG_007530.1:g.102205_102206delinsCT , LRG_754:g.102205_102206delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083-34_1083-33delinsCT
ENST00000685279.1:c.-31-34_-31-33delinsCT	ENSP00000509424.1:n.-31-34_-31-33delinsCT
ENST00000688043.1:n.1424-34_1424-33delinsCT
ENST00000689668.1:n.1210-34_1210-33delinsCT
ENST00000690679.1:c.1390-34_1390-33delinsCT
ENST00000690876.1:c.1092-34_1092-33delinsCT	ENSP00000508955.1:n.1092-34_1092-33delinsCT
ENST00000691229.1:c.1092-34_1092-33delinsCT	ENSP00000510437.1:n.1092-34_1092-33delinsCT
ENST00000692089.1:c.1092-34_1092-33delinsCT	ENSP00000508626.1:n.1092-34_1092-33delinsCT
ENST00000692620.1:c.-31-34_-31-33delinsCT	ENSP00000509311.1:n.-31-34_-31-33delinsCT
ENST00000402219.8:c.1203-34_1203-33delinsCT MANE Select	ENSP00000384675.2:n.1203-34_1203-33delinsCT
ENST00000395038.6:c.1203-34_1203-33delinsCT	ENSP00000378479.2:n.1203-34_1203-33delinsCT
ENST00000402219.6:c.1203-34_1203-33delinsCT	ENSP00000384675.2:n.1203-34_1203-33delinsCT
ENST00000426016.5:c.1203-34_1203-33delinsCT	ENSP00000387784.1:n.1203-34_1203-33delinsCT
ENST00000472480.1:n.47-34_47-33delinsCT
NM_005633.3:c.1203-34_1203-33delinsCT , LRG_754t1:c.1203-34_1203-33delinsCT	NP_005624.2:n.1203-34_1203-33delinsCT
XM_005264515.3:c.1203-34_1203-33delinsCT	XP_005264572.1:n.1203-34_1203-33delinsCT
XM_011533060.1:c.1296-34_1296-33delinsCT	XP_011531362.1:n.1296-34_1296-33delinsCT
XM_011533061.1:c.1296-34_1296-33delinsCT	XP_011531363.1:n.1296-34_1296-33delinsCT
XM_011533062.1:c.1182-34_1182-33delinsCT	XP_011531364.1:n.1182-34_1182-33delinsCT
XM_011533063.1:c.1179-34_1179-33delinsCT	XP_011531365.1:n.1179-34_1179-33delinsCT
XM_011533064.1:c.1032-34_1032-33delinsCT	XP_011531366.1:n.1032-34_1032-33delinsCT
XM_011533065.1:c.1296-34_1296-33delinsCT	XP_011531367.1:n.1296-34_1296-33delinsCT
XM_011533066.1:c.138-34_138-33delinsCT	XP_011531368.1:n.138-34_138-33delinsCT
XM_005264515.4:c.1203-34_1203-33delinsCT	XP_005264572.1:n.1203-34_1203-33delinsCT
XM_011533062.2:c.1182-34_1182-33delinsCT	XP_011531364.1:n.1182-34_1182-33delinsCT
XM_011533064.2:c.1032-34_1032-33delinsCT	XP_011531366.1:n.1032-34_1032-33delinsCT
NM_001382394.1:c.1182-34_1182-33delinsCT	NP_001369323.1:n.1182-34_1182-33delinsCT
NM_001382395.1:c.1203-34_1203-33delinsCT	NP_001369324.1:n.1203-34_1203-33delinsCT
NM_005633.4:c.1203-34_1203-33delinsCT MANE Select	NP_005624.2:n.1203-34_1203-33delinsCT