Canonical Allele Identifier: CA297270
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 181552
ClinVar RCV Id: RCV000159168 RCV003224178
dbSNP Id: rs730881044
MyVariant Identifiers: chr2:g.39250139T>C (hg19) chr2:g.39022998T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022998T>C , CM000664.2:g.39022998T>C GRCh38
NC_000002.11:g.39250139T>C , CM000664.1:g.39250139T>C GRCh37
NC_000002.10:g.39103643T>C NCBI36
NG_007530.1:g.102466A>G , LRG_754:g.102466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1310A>G
ENST00000685279.1:c.197A>G ENSP00000509424.1:p.Gln66Arg
ENST00000688043.1:n.1651A>G
ENST00000689668.1:n.1437A>G
ENST00000690876.1:c.1319A>G ENSP00000508955.1:p.Gln440Arg
ENST00000691229.1:c.1319A>G ENSP00000510437.1:p.Gln440Arg
ENST00000692089.1:c.1319A>G ENSP00000508626.1:p.Gln440Arg
ENST00000692620.1:c.197A>G ENSP00000509311.1:p.Gln66Arg
ENST00000402219.8:c.1430A>G MANE Select ENSP00000384675.2:p.Gln477Arg
ENST00000395038.6:c.1430A>G ENSP00000378479.2:p.Gln477Arg
ENST00000402219.6:c.1430A>G ENSP00000384675.2:p.Gln477Arg
ENST00000426016.5:c.1430A>G ENSP00000387784.1:p.Gln477Arg
ENST00000472480.1:n.274A>G
NM_005633.3:c.1430A>G , LRG_754t1:c.1430A>G NP_005624.2:p.Gln477Arg
XM_005264515.3:c.1430A>G XP_005264572.1:p.Gln477Arg
XM_011533060.1:c.1523A>G XP_011531362.1:p.Gln508Arg
XM_011533061.1:c.1523A>G XP_011531363.1:p.Gln508Arg
XM_011533062.1:c.1409A>G XP_011531364.1:p.Gln470Arg
XM_011533063.1:c.1406A>G XP_011531365.1:p.Gln469Arg
XM_011533064.1:c.1259A>G XP_011531366.1:p.Gln420Arg
XM_011533065.1:c.1523A>G XP_011531367.1:p.Gln508Arg
XM_011533066.1:c.365A>G XP_011531368.1:p.Gln122Arg
XM_005264515.4:c.1430A>G XP_005264572.1:p.Gln477Arg
XM_011533062.2:c.1409A>G XP_011531364.1:p.Gln470Arg
XM_011533064.2:c.1259A>G XP_011531366.1:p.Gln420Arg
NM_001382394.1:c.1409A>G NP_001369323.1:p.Gln470Arg
NM_001382395.1:c.1430A>G NP_001369324.1:p.Gln477Arg
NM_005633.4:c.1430A>G MANE Select NP_005624.2:p.Gln477Arg
Search 100 bp 5'
Search 100 bp 3'