Canonical Allele Identifier: CA1246153912
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054698A= , CM000664.2:g.39054698A= GRCh38
NC_000002.11:g.39281839A= , CM000664.1:g.39281839A= GRCh37
NC_000002.10:g.39135343A= NCBI36
NG_007530.1:g.70766T= , LRG_754:g.70766T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.663T=
ENST00000685782.1:n.1474T=
ENST00000688189.1:n.401T=
ENST00000689668.1:n.643T=
ENST00000690679.1:c.736T=
ENST00000690876.1:c.636T= ENSP00000508955.1:p.Ile212=
ENST00000691229.1:c.636T= ENSP00000510437.1:p.Ile212=
ENST00000692089.1:c.636T= ENSP00000508626.1:p.Ile212=
ENST00000402219.8:c.636T= MANE Select ENSP00000384675.2:p.Ile212=
ENST00000395038.6:c.636T= ENSP00000378479.2:p.Ile212=
ENST00000402219.6:c.636T= ENSP00000384675.2:p.Ile212=
ENST00000426016.5:c.636T= ENSP00000387784.1:p.Ile212=
NM_005633.3:c.636T= , LRG_754t1:c.636T= NP_005624.2:p.Ile212=
XM_005264515.3:c.636T= XP_005264572.1:p.Ile212=
XM_011533060.1:c.729T= XP_011531362.1:p.Ile243=
XM_011533061.1:c.729T= XP_011531363.1:p.Ile243=
XM_011533062.1:c.615T= XP_011531364.1:p.Ile205=
XM_011533063.1:c.612T= XP_011531365.1:p.Ile204=
XM_011533064.1:c.465T= XP_011531366.1:p.Ile155=
XM_011533065.1:c.729T= XP_011531367.1:p.Ile243=
XM_005264515.4:c.636T= XP_005264572.1:p.Ile212=
XM_011533062.2:c.615T= XP_011531364.1:p.Ile205=
XM_011533064.2:c.465T= XP_011531366.1:p.Ile155=
NM_001382394.1:c.615T= NP_001369323.1:p.Ile205=
NM_001382395.1:c.636T= NP_001369324.1:p.Ile212=
NM_005633.4:c.636T= MANE Select NP_005624.2:p.Ile212=