Canonical Allele Identifier: CA1246140242

Gene: SOS1

Linked Data

• dbSNP Id: rs1669857617
• gnomAD v4: 2-39023352-ATAGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023357_39023361del , CM000664.2:g.39023357_39023361del	GRCh38
NC_000002.11:g.39250498_39250502del , CM000664.1:g.39250498_39250502del	GRCh37
NC_000002.10:g.39104002_39104006del	NCBI36
NG_007530.1:g.102107_102111del , LRG_754:g.102107_102111del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083-132_1083-128del
ENST00000685279.1:c.-31-132_-31-128del	ENSP00000509424.1:n.-31-132_-31-128del
ENST00000688043.1:n.1424-132_1424-128del
ENST00000689668.1:n.1210-132_1210-128del
ENST00000690679.1:c.1390-132_1390-128del
ENST00000690876.1:c.1092-132_1092-128del	ENSP00000508955.1:n.1092-132_1092-128del
ENST00000691229.1:c.1092-132_1092-128del	ENSP00000510437.1:n.1092-132_1092-128del
ENST00000692089.1:c.1092-132_1092-128del	ENSP00000508626.1:n.1092-132_1092-128del
ENST00000692620.1:c.-31-132_-31-128del	ENSP00000509311.1:n.-31-132_-31-128del
ENST00000402219.8:c.1203-132_1203-128del MANE Select	ENSP00000384675.2:n.1203-132_1203-128del
ENST00000395038.6:c.1203-132_1203-128del	ENSP00000378479.2:n.1203-132_1203-128del
ENST00000402219.6:c.1203-132_1203-128del	ENSP00000384675.2:n.1203-132_1203-128del
ENST00000426016.5:c.1203-132_1203-128del	ENSP00000387784.1:n.1203-132_1203-128del
ENST00000472480.1:n.47-132_47-128del
NM_005633.3:c.1203-132_1203-128del , LRG_754t1:c.1203-132_1203-128del	NP_005624.2:n.1203-132_1203-128del
XM_005264515.3:c.1203-132_1203-128del	XP_005264572.1:n.1203-132_1203-128del
XM_011533060.1:c.1296-132_1296-128del	XP_011531362.1:n.1296-132_1296-128del
XM_011533061.1:c.1296-132_1296-128del	XP_011531363.1:n.1296-132_1296-128del
XM_011533062.1:c.1182-132_1182-128del	XP_011531364.1:n.1182-132_1182-128del
XM_011533063.1:c.1179-132_1179-128del	XP_011531365.1:n.1179-132_1179-128del
XM_011533064.1:c.1032-132_1032-128del	XP_011531366.1:n.1032-132_1032-128del
XM_011533065.1:c.1296-132_1296-128del	XP_011531367.1:n.1296-132_1296-128del
XM_011533066.1:c.138-132_138-128del	XP_011531368.1:n.138-132_138-128del
XM_005264515.4:c.1203-132_1203-128del	XP_005264572.1:n.1203-132_1203-128del
XM_011533062.2:c.1182-132_1182-128del	XP_011531364.1:n.1182-132_1182-128del
XM_011533064.2:c.1032-132_1032-128del	XP_011531366.1:n.1032-132_1032-128del
NM_001382394.1:c.1182-132_1182-128del	NP_001369323.1:n.1182-132_1182-128del
NM_001382395.1:c.1203-132_1203-128del	NP_001369324.1:n.1203-132_1203-128del
NM_005633.4:c.1203-132_1203-128del MANE Select	NP_005624.2:n.1203-132_1203-128del