Canonical Allele Identifier: CA2658715532
Gene: SOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39023310_39023311insCTAC , CM000664.2:g.39023310_39023311insCTAC GRCh38
NC_000002.11:g.39250451_39250452insCTAC , CM000664.1:g.39250451_39250452insCTAC GRCh37
NC_000002.10:g.39103955_39103956insCTAC NCBI36
NG_007530.1:g.102153_102154insGTAG , LRG_754:g.102153_102154insGTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1083-86_1083-85insGTAG
ENST00000685279.1:c.-31-86_-31-85insGTAG ENSP00000509424.1:n.-31-86_-31-85insGTAG
ENST00000688043.1:n.1424-86_1424-85insGTAG
ENST00000689668.1:n.1210-86_1210-85insGTAG
ENST00000690679.1:c.1390-86_1390-85insGTAG
ENST00000690876.1:c.1092-86_1092-85insGTAG ENSP00000508955.1:n.1092-86_1092-85insGTAG
ENST00000691229.1:c.1092-86_1092-85insGTAG ENSP00000510437.1:n.1092-86_1092-85insGTAG
ENST00000692089.1:c.1092-86_1092-85insGTAG ENSP00000508626.1:n.1092-86_1092-85insGTAG
ENST00000692620.1:c.-31-86_-31-85insGTAG ENSP00000509311.1:n.-31-86_-31-85insGTAG
ENST00000402219.8:c.1203-86_1203-85insGTAG MANE Select ENSP00000384675.2:n.1203-86_1203-85insGTAG
ENST00000395038.6:c.1203-86_1203-85insGTAG ENSP00000378479.2:n.1203-86_1203-85insGTAG
ENST00000402219.6:c.1203-86_1203-85insGTAG ENSP00000384675.2:n.1203-86_1203-85insGTAG
ENST00000426016.5:c.1203-86_1203-85insGTAG ENSP00000387784.1:n.1203-86_1203-85insGTAG
ENST00000472480.1:n.47-86_47-85insGTAG
NM_005633.3:c.1203-86_1203-85insGTAG , LRG_754t1:c.1203-86_1203-85insGTAG NP_005624.2:n.1203-86_1203-85insGTAG
XM_005264515.3:c.1203-86_1203-85insGTAG XP_005264572.1:n.1203-86_1203-85insGTAG
XM_011533060.1:c.1296-86_1296-85insGTAG XP_011531362.1:n.1296-86_1296-85insGTAG
XM_011533061.1:c.1296-86_1296-85insGTAG XP_011531363.1:n.1296-86_1296-85insGTAG
XM_011533062.1:c.1182-86_1182-85insGTAG XP_011531364.1:n.1182-86_1182-85insGTAG
XM_011533063.1:c.1179-86_1179-85insGTAG XP_011531365.1:n.1179-86_1179-85insGTAG
XM_011533064.1:c.1032-86_1032-85insGTAG XP_011531366.1:n.1032-86_1032-85insGTAG
XM_011533065.1:c.1296-86_1296-85insGTAG XP_011531367.1:n.1296-86_1296-85insGTAG
XM_011533066.1:c.138-86_138-85insGTAG XP_011531368.1:n.138-86_138-85insGTAG
XM_005264515.4:c.1203-86_1203-85insGTAG XP_005264572.1:n.1203-86_1203-85insGTAG
XM_011533062.2:c.1182-86_1182-85insGTAG XP_011531364.1:n.1182-86_1182-85insGTAG
XM_011533064.2:c.1032-86_1032-85insGTAG XP_011531366.1:n.1032-86_1032-85insGTAG
NM_001382394.1:c.1182-86_1182-85insGTAG NP_001369323.1:n.1182-86_1182-85insGTAG
NM_001382395.1:c.1203-86_1203-85insGTAG NP_001369324.1:n.1203-86_1203-85insGTAG
NM_005633.4:c.1203-86_1203-85insGTAG MANE Select NP_005624.2:n.1203-86_1203-85insGTAG