Canonical Allele Identifier: CA2586964760
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022995_39022997delinsAGA , CM000664.2:g.39022995_39022997delinsAGA GRCh38
NC_000002.11:g.39250136_39250138delinsAGA , CM000664.1:g.39250136_39250138delinsAGA GRCh37
NC_000002.10:g.39103640_39103642delinsAGA NCBI36
NG_007530.1:g.102467_102469delinsTCT , LRG_754:g.102467_102469delinsTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1311_1313delinsTCT
ENST00000685279.1:c.198_200delinsTCT ENSP00000509424.1:p.Gln66_Pro67delinsHisLeu
ENST00000688043.1:n.1652_1654delinsTCT
ENST00000689668.1:n.1438_1440delinsTCT
ENST00000690876.1:c.1320_1322delinsTCT ENSP00000508955.1:p.Gln440_Pro441delinsHisLeu
ENST00000691229.1:c.1320_1322delinsTCT ENSP00000510437.1:p.Gln440_Pro441delinsHisLeu
ENST00000692089.1:c.1320_1322delinsTCT ENSP00000508626.1:p.Gln440_Pro441delinsHisLeu
ENST00000692620.1:c.198_200delinsTCT ENSP00000509311.1:p.Gln66_Pro67delinsHisLeu
ENST00000402219.8:c.1431_1433delinsTCT MANE Select ENSP00000384675.2:p.Gln477_Pro478delinsHisLeu
ENST00000395038.6:c.1431_1433delinsTCT ENSP00000378479.2:p.Gln477_Pro478delinsHisLeu
ENST00000402219.6:c.1431_1433delinsTCT ENSP00000384675.2:p.Gln477_Pro478delinsHisLeu
ENST00000426016.5:c.1431_1433delinsTCT ENSP00000387784.1:p.Gln477_Pro478delinsHisLeu
ENST00000472480.1:n.275_277delinsTCT
NM_005633.3:c.1431_1433delinsTCT , LRG_754t1:c.1431_1433delinsTCT NP_005624.2:p.Gln477_Pro478delinsHisLeu
XM_005264515.3:c.1431_1433delinsTCT XP_005264572.1:p.Gln477_Pro478delinsHisLeu
XM_011533060.1:c.1524_1526delinsTCT XP_011531362.1:p.Gln508_Pro509delinsHisLeu
XM_011533061.1:c.1524_1526delinsTCT XP_011531363.1:p.Gln508_Pro509delinsHisLeu
XM_011533062.1:c.1410_1412delinsTCT XP_011531364.1:p.Gln470_Pro471delinsHisLeu
XM_011533063.1:c.1407_1409delinsTCT XP_011531365.1:p.Gln469_Pro470delinsHisLeu
XM_011533064.1:c.1260_1262delinsTCT XP_011531366.1:p.Gln420_Pro421delinsHisLeu
XM_011533065.1:c.1524_1526delinsTCT XP_011531367.1:p.Gln508_Pro509delinsHisLeu
XM_011533066.1:c.366_368delinsTCT XP_011531368.1:p.Gln122_Pro123delinsHisLeu
XM_005264515.4:c.1431_1433delinsTCT XP_005264572.1:p.Gln477_Pro478delinsHisLeu
XM_011533062.2:c.1410_1412delinsTCT XP_011531364.1:p.Gln470_Pro471delinsHisLeu
XM_011533064.2:c.1260_1262delinsTCT XP_011531366.1:p.Gln420_Pro421delinsHisLeu
NM_001382394.1:c.1410_1412delinsTCT NP_001369323.1:p.Gln470_Pro471delinsHisLeu
NM_001382395.1:c.1431_1433delinsTCT NP_001369324.1:p.Gln477_Pro478delinsHisLeu
NM_005633.4:c.1431_1433delinsTCT MANE Select NP_005624.2:p.Gln477_Pro478delinsHisLeu