Canonical Allele Identifier: CA1246131856
Community Standard Title: NM_005633.4(SOS1):c.2167+15_2167+17delinsTTA
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39013443_39013445delinsTAA , CM000664.2:g.39013443_39013445delinsTAA GRCh38
NC_000002.11:g.39240584_39240586delinsTAA , CM000664.1:g.39240584_39240586delinsTAA GRCh37
NC_000002.10:g.39094088_39094090delinsTAA NCBI36
NG_007530.1:g.112019_112021delinsTTA , LRG_754:g.112019_112021delinsTTA

Transcript Alleles

HGVS Amino-acid Change
NM_005633.4:c.2167+15_2167+17delinsTTA MANE Select NP_005624.2:n.2167+15_2167+17delinsTTA
ENST00000402219.8:c.2167+15_2167+17delinsTTA MANE Select ENSP00000384675.2:n.2167+15_2167+17delinsTTA
NM_001382394.1:c.2146+15_2146+17delinsTTA NP_001369323.1:n.2146+15_2146+17delinsTTA
NM_001382395.1:c.2167+15_2167+17delinsTTA NP_001369324.1:n.2167+15_2167+17delinsTTA
NM_005633.3:c.2167+15_2167+17delinsTTA , LRG_754t1:c.2167+15_2167+17delinsTTA NP_005624.2:n.2167+15_2167+17delinsTTA
ENST00000395038.6:c.2167+15_2167+17delinsTTA ENSP00000378479.2:n.2167+15_2167+17delinsTTA
ENST00000402219.6:c.2167+15_2167+17delinsTTA ENSP00000384675.2:n.2167+15_2167+17delinsTTA
ENST00000426016.5:c.2167+15_2167+17delinsTTA ENSP00000387784.1:n.2167+15_2167+17delinsTTA
ENST00000685279.1:c.934+15_934+17delinsTTA ENSP00000509424.1:n.934+15_934+17delinsTTA
ENST00000688043.1:n.2403_2405delinsTTA
ENST00000689668.1:n.2174+15_2174+17delinsTTA
ENST00000690514.1:n.256+15_256+17delinsTTA
ENST00000690876.1:c.2056+15_2056+17delinsTTA ENSP00000508955.1:n.2056+15_2056+17delinsTTA
ENST00000691229.1:c.2056+15_2056+17delinsTTA ENSP00000510437.1:n.2056+15_2056+17delinsTTA
ENST00000692089.1:c.2056+15_2056+17delinsTTA ENSP00000508626.1:n.2056+15_2056+17delinsTTA
ENST00000692620.1:c.934+15_934+17delinsTTA ENSP00000509311.1:n.934+15_934+17delinsTTA
XM_005264515.3:c.2167+15_2167+17delinsTTA XP_005264572.1:n.2167+15_2167+17delinsTTA
XM_005264515.4:c.2167+15_2167+17delinsTTA XP_005264572.1:n.2167+15_2167+17delinsTTA
XM_011533060.1:c.2260+15_2260+17delinsTTA XP_011531362.1:n.2260+15_2260+17delinsTTA
XM_011533061.1:c.2260+15_2260+17delinsTTA XP_011531363.1:n.2260+15_2260+17delinsTTA
XM_011533062.1:c.2146+15_2146+17delinsTTA XP_011531364.1:n.2146+15_2146+17delinsTTA
XM_011533062.2:c.2146+15_2146+17delinsTTA XP_011531364.1:n.2146+15_2146+17delinsTTA
XM_011533063.1:c.2143+15_2143+17delinsTTA XP_011531365.1:n.2143+15_2143+17delinsTTA
XM_011533064.1:c.1996+15_1996+17delinsTTA XP_011531366.1:n.1996+15_1996+17delinsTTA
XM_011533064.2:c.1996+15_1996+17delinsTTA XP_011531366.1:n.1996+15_1996+17delinsTTA
XM_011533065.1:c.2260+15_2260+17delinsTTA XP_011531367.1:n.2260+15_2260+17delinsTTA
XM_011533066.1:c.1102+15_1102+17delinsTTA XP_011531368.1:n.1102+15_1102+17delinsTTA