Canonical Allele Identifier: CA1246139320
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022696_39022697delinsCA , CM000664.2:g.39022696_39022697delinsCA GRCh38
NC_000002.11:g.39249837_39249838delinsCA , CM000664.1:g.39249837_39249838delinsCA GRCh37
NC_000002.10:g.39103341_39103342delinsCA NCBI36
NG_007530.1:g.102767_102768delinsTG , LRG_754:g.102767_102768delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1611_1612delinsTG
ENST00000685279.1:c.498_499delinsTG ENSP00000509424.1:p.Phe166=
ENST00000688043.1:n.1952_1953delinsTG
ENST00000689668.1:n.1738_1739delinsTG
ENST00000690876.1:c.1620_1621delinsTG ENSP00000508955.1:p.Phe540=
ENST00000691229.1:c.1620_1621delinsTG ENSP00000510437.1:p.Phe540=
ENST00000692089.1:c.1620_1621delinsTG ENSP00000508626.1:p.Phe540=
ENST00000692620.1:c.498_499delinsTG ENSP00000509311.1:p.Phe166=
ENST00000402219.8:c.1731_1732delinsTG MANE Select ENSP00000384675.2:p.Phe577=
ENST00000395038.6:c.1731_1732delinsTG ENSP00000378479.2:p.Phe577=
ENST00000402219.6:c.1731_1732delinsTG ENSP00000384675.2:p.Phe577=
ENST00000426016.5:c.1731_1732delinsTG ENSP00000387784.1:p.Phe577=
NM_005633.3:c.1731_1732delinsTG , LRG_754t1:c.1731_1732delinsTG NP_005624.2:p.Phe577=
XM_005264515.3:c.1731_1732delinsTG XP_005264572.1:p.Phe577=
XM_011533060.1:c.1824_1825delinsTG XP_011531362.1:p.Phe608=
XM_011533061.1:c.1824_1825delinsTG XP_011531363.1:p.Phe608=
XM_011533062.1:c.1710_1711delinsTG XP_011531364.1:p.Phe570=
XM_011533063.1:c.1707_1708delinsTG XP_011531365.1:p.Phe569=
XM_011533064.1:c.1560_1561delinsTG XP_011531366.1:p.Phe520=
XM_011533065.1:c.1824_1825delinsTG XP_011531367.1:p.Phe608=
XM_011533066.1:c.666_667delinsTG XP_011531368.1:p.Phe222=
XM_005264515.4:c.1731_1732delinsTG XP_005264572.1:p.Phe577=
XM_011533062.2:c.1710_1711delinsTG XP_011531364.1:p.Phe570=
XM_011533064.2:c.1560_1561delinsTG XP_011531366.1:p.Phe520=
NM_001382394.1:c.1710_1711delinsTG NP_001369323.1:p.Phe570=
NM_001382395.1:c.1731_1732delinsTG NP_001369324.1:p.Phe577=
NM_005633.4:c.1731_1732delinsTG MANE Select NP_005624.2:p.Phe577=