Canonical Allele Identifier: CA1246140226

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023316_39023317delinsCA , CM000664.2:g.39023316_39023317delinsCA	GRCh38
NC_000002.11:g.39250457_39250458delinsCA , CM000664.1:g.39250457_39250458delinsCA	GRCh37
NC_000002.10:g.39103961_39103962delinsCA	NCBI36
NG_007530.1:g.102147_102148delinsTG , LRG_754:g.102147_102148delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083-92_1083-91delinsTG
ENST00000685279.1:c.-31-92_-31-91delinsTG	ENSP00000509424.1:n.-31-92_-31-91delinsTG
ENST00000688043.1:n.1424-92_1424-91delinsTG
ENST00000689668.1:n.1210-92_1210-91delinsTG
ENST00000690679.1:c.1390-92_1390-91delinsTG
ENST00000690876.1:c.1092-92_1092-91delinsTG	ENSP00000508955.1:n.1092-92_1092-91delinsTG
ENST00000691229.1:c.1092-92_1092-91delinsTG	ENSP00000510437.1:n.1092-92_1092-91delinsTG
ENST00000692089.1:c.1092-92_1092-91delinsTG	ENSP00000508626.1:n.1092-92_1092-91delinsTG
ENST00000692620.1:c.-31-92_-31-91delinsTG	ENSP00000509311.1:n.-31-92_-31-91delinsTG
ENST00000402219.8:c.1203-92_1203-91delinsTG MANE Select	ENSP00000384675.2:n.1203-92_1203-91delinsTG
ENST00000395038.6:c.1203-92_1203-91delinsTG	ENSP00000378479.2:n.1203-92_1203-91delinsTG
ENST00000402219.6:c.1203-92_1203-91delinsTG	ENSP00000384675.2:n.1203-92_1203-91delinsTG
ENST00000426016.5:c.1203-92_1203-91delinsTG	ENSP00000387784.1:n.1203-92_1203-91delinsTG
ENST00000472480.1:n.47-92_47-91delinsTG
NM_005633.3:c.1203-92_1203-91delinsTG , LRG_754t1:c.1203-92_1203-91delinsTG	NP_005624.2:n.1203-92_1203-91delinsTG
XM_005264515.3:c.1203-92_1203-91delinsTG	XP_005264572.1:n.1203-92_1203-91delinsTG
XM_011533060.1:c.1296-92_1296-91delinsTG	XP_011531362.1:n.1296-92_1296-91delinsTG
XM_011533061.1:c.1296-92_1296-91delinsTG	XP_011531363.1:n.1296-92_1296-91delinsTG
XM_011533062.1:c.1182-92_1182-91delinsTG	XP_011531364.1:n.1182-92_1182-91delinsTG
XM_011533063.1:c.1179-92_1179-91delinsTG	XP_011531365.1:n.1179-92_1179-91delinsTG
XM_011533064.1:c.1032-92_1032-91delinsTG	XP_011531366.1:n.1032-92_1032-91delinsTG
XM_011533065.1:c.1296-92_1296-91delinsTG	XP_011531367.1:n.1296-92_1296-91delinsTG
XM_011533066.1:c.138-92_138-91delinsTG	XP_011531368.1:n.138-92_138-91delinsTG
XM_005264515.4:c.1203-92_1203-91delinsTG	XP_005264572.1:n.1203-92_1203-91delinsTG
XM_011533062.2:c.1182-92_1182-91delinsTG	XP_011531364.1:n.1182-92_1182-91delinsTG
XM_011533064.2:c.1032-92_1032-91delinsTG	XP_011531366.1:n.1032-92_1032-91delinsTG
NM_001382394.1:c.1182-92_1182-91delinsTG	NP_001369323.1:n.1182-92_1182-91delinsTG
NM_001382395.1:c.1203-92_1203-91delinsTG	NP_001369324.1:n.1203-92_1203-91delinsTG
NM_005633.4:c.1203-92_1203-91delinsTG MANE Select	NP_005624.2:n.1203-92_1203-91delinsTG