Canonical Allele Identifier: CA1139532821
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806113
ClinVar RCV Id: RCV002470397

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39023034_39023035delinsAA , CM000664.2:g.39023034_39023035delinsAA GRCh38
NC_000002.11:g.39250175_39250176delinsAA , CM000664.1:g.39250175_39250176delinsAA GRCh37
NC_000002.10:g.39103679_39103680delinsAA NCBI36
NG_007530.1:g.102429_102430delinsTT , LRG_754:g.102429_102430delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1273_1274delinsTT
ENST00000685279.1:c.160_161delinsTT ENSP00000509424.1:p.Asp54Phe
ENST00000688043.1:n.1614_1615delinsTT
ENST00000689668.1:n.1400_1401delinsTT
ENST00000690876.1:c.1282_1283delinsTT ENSP00000508955.1:p.Asp428Phe
ENST00000691229.1:c.1282_1283delinsTT ENSP00000510437.1:p.Asp428Phe
ENST00000692089.1:c.1282_1283delinsTT ENSP00000508626.1:p.Asp428Phe
ENST00000692620.1:c.160_161delinsTT ENSP00000509311.1:p.Asp54Phe
ENST00000402219.8:c.1393_1394delinsTT MANE Select ENSP00000384675.2:p.Asp465Phe
ENST00000395038.6:c.1393_1394delinsTT ENSP00000378479.2:p.Asp465Phe
ENST00000402219.6:c.1393_1394delinsTT ENSP00000384675.2:p.Asp465Phe
ENST00000426016.5:c.1393_1394delinsTT ENSP00000387784.1:p.Asp465Phe
ENST00000472480.1:n.237_238delinsTT
NM_005633.3:c.1393_1394delinsTT , LRG_754t1:c.1393_1394delinsTT NP_005624.2:p.Asp465Phe
XM_005264515.3:c.1393_1394delinsTT XP_005264572.1:p.Asp465Phe
XM_011533060.1:c.1486_1487delinsTT XP_011531362.1:p.Asp496Phe
XM_011533061.1:c.1486_1487delinsTT XP_011531363.1:p.Asp496Phe
XM_011533062.1:c.1372_1373delinsTT XP_011531364.1:p.Asp458Phe
XM_011533063.1:c.1369_1370delinsTT XP_011531365.1:p.Asp457Phe
XM_011533064.1:c.1222_1223delinsTT XP_011531366.1:p.Asp408Phe
XM_011533065.1:c.1486_1487delinsTT XP_011531367.1:p.Asp496Phe
XM_011533066.1:c.328_329delinsTT XP_011531368.1:p.Asp110Phe
XM_005264515.4:c.1393_1394delinsTT XP_005264572.1:p.Asp465Phe
XM_011533062.2:c.1372_1373delinsTT XP_011531364.1:p.Asp458Phe
XM_011533064.2:c.1222_1223delinsTT XP_011531366.1:p.Asp408Phe
NM_001382394.1:c.1372_1373delinsTT NP_001369323.1:p.Asp458Phe
NM_001382395.1:c.1393_1394delinsTT NP_001369324.1:p.Asp465Phe
NM_005633.4:c.1393_1394delinsTT MANE Select NP_005624.2:p.Asp465Phe