Canonical Allele Identifier: CA346365610
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312787
dbSNP Id: rs1386900583
gnomAD v2: 2-39249879-C-T
gnomAD v4: 2-39022738-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022738C>T , CM000664.2:g.39022738C>T GRCh38
NC_000002.11:g.39249879C>T , CM000664.1:g.39249879C>T GRCh37
NC_000002.10:g.39103383C>T NCBI36
NG_007530.1:g.102726G>A , LRG_754:g.102726G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1570G>A
ENST00000685279.1:c.457G>A ENSP00000509424.1:p.Glu153Lys
ENST00000688043.1:n.1911G>A
ENST00000689668.1:n.1697G>A
ENST00000690876.1:c.1579G>A ENSP00000508955.1:p.Glu527Lys
ENST00000691229.1:c.1579G>A ENSP00000510437.1:p.Glu527Lys
ENST00000692089.1:c.1579G>A ENSP00000508626.1:p.Glu527Lys
ENST00000692620.1:c.457G>A ENSP00000509311.1:p.Glu153Lys
ENST00000402219.8:c.1690G>A MANE Select ENSP00000384675.2:p.Glu564Lys
ENST00000395038.6:c.1690G>A ENSP00000378479.2:p.Glu564Lys
ENST00000402219.6:c.1690G>A ENSP00000384675.2:p.Glu564Lys
ENST00000426016.5:c.1690G>A ENSP00000387784.1:p.Glu564Lys
NM_005633.3:c.1690G>A , LRG_754t1:c.1690G>A NP_005624.2:p.Glu564Lys
XM_005264515.3:c.1690G>A XP_005264572.1:p.Glu564Lys
XM_011533060.1:c.1783G>A XP_011531362.1:p.Glu595Lys
XM_011533061.1:c.1783G>A XP_011531363.1:p.Glu595Lys
XM_011533062.1:c.1669G>A XP_011531364.1:p.Glu557Lys
XM_011533063.1:c.1666G>A XP_011531365.1:p.Glu556Lys
XM_011533064.1:c.1519G>A XP_011531366.1:p.Glu507Lys
XM_011533065.1:c.1783G>A XP_011531367.1:p.Glu595Lys
XM_011533066.1:c.625G>A XP_011531368.1:p.Glu209Lys
XM_005264515.4:c.1690G>A XP_005264572.1:p.Glu564Lys
XM_011533062.2:c.1669G>A XP_011531364.1:p.Glu557Lys
XM_011533064.2:c.1519G>A XP_011531366.1:p.Glu507Lys
NM_001382394.1:c.1669G>A NP_001369323.1:p.Glu557Lys
NM_001382395.1:c.1690G>A NP_001369324.1:p.Glu564Lys
NM_005633.4:c.1690G>A MANE Select NP_005624.2:p.Glu564Lys