Canonical Allele Identifier: CA346372946
Gene: SOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054634A>G , CM000664.2:g.39054634A>G GRCh38
NC_000002.11:g.39281775A>G , CM000664.1:g.39281775A>G GRCh37
NC_000002.10:g.39135279A>G NCBI36
NG_007530.1:g.70830T>C , LRG_754:g.70830T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.727T>C
ENST00000685782.1:n.1538T>C
ENST00000688189.1:n.465T>C
ENST00000689668.1:n.707T>C
ENST00000690679.1:c.800T>C
ENST00000690876.1:c.700T>C ENSP00000508955.1:p.Ser234Pro
ENST00000691229.1:c.700T>C ENSP00000510437.1:p.Ser234Pro
ENST00000692089.1:c.700T>C ENSP00000508626.1:p.Ser234Pro
ENST00000402219.8:c.700T>C MANE Select ENSP00000384675.2:p.Ser234Pro
ENST00000395038.6:c.700T>C ENSP00000378479.2:p.Ser234Pro
ENST00000402219.6:c.700T>C ENSP00000384675.2:p.Ser234Pro
ENST00000426016.5:c.700T>C ENSP00000387784.1:p.Ser234Pro
NM_005633.3:c.700T>C , LRG_754t1:c.700T>C NP_005624.2:p.Ser234Pro
XM_005264515.3:c.700T>C XP_005264572.1:p.Ser234Pro
XM_011533060.1:c.793T>C XP_011531362.1:p.Ser265Pro
XM_011533061.1:c.793T>C XP_011531363.1:p.Ser265Pro
XM_011533062.1:c.679T>C XP_011531364.1:p.Ser227Pro
XM_011533063.1:c.676T>C XP_011531365.1:p.Ser226Pro
XM_011533064.1:c.529T>C XP_011531366.1:p.Ser177Pro
XM_011533065.1:c.793T>C XP_011531367.1:p.Ser265Pro
XM_005264515.4:c.700T>C XP_005264572.1:p.Ser234Pro
XM_011533062.2:c.679T>C XP_011531364.1:p.Ser227Pro
XM_011533064.2:c.529T>C XP_011531366.1:p.Ser177Pro
NM_001382394.1:c.679T>C NP_001369323.1:p.Ser227Pro
NM_001382395.1:c.700T>C NP_001369324.1:p.Ser234Pro
NM_005633.4:c.700T>C MANE Select NP_005624.2:p.Ser234Pro