Canonical Allele Identifier: CA425866706
Gene: SOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.39249808T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022667T>G , CM000664.2:g.39022667T>G GRCh38
NC_000002.11:g.39249808T>G , CM000664.1:g.39249808T>G GRCh37
NC_000002.10:g.39103312T>G NCBI36
NG_007530.1:g.102797A>C , LRG_754:g.102797A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1641A>C
ENST00000685279.1:c.528A>C ENSP00000509424.1:p.Ile176=
ENST00000688043.1:n.1982A>C
ENST00000689668.1:n.1768A>C
ENST00000690876.1:c.1650A>C ENSP00000508955.1:p.Ile550=
ENST00000691229.1:c.1650A>C ENSP00000510437.1:p.Ile550=
ENST00000692089.1:c.1650A>C ENSP00000508626.1:p.Ile550=
ENST00000692620.1:c.528A>C ENSP00000509311.1:p.Ile176=
ENST00000402219.8:c.1761A>C MANE Select ENSP00000384675.2:p.Ile587=
ENST00000395038.6:c.1761A>C ENSP00000378479.2:p.Ile587=
ENST00000402219.6:c.1761A>C ENSP00000384675.2:p.Ile587=
ENST00000426016.5:c.1761A>C ENSP00000387784.1:p.Ile587=
NM_005633.3:c.1761A>C , LRG_754t1:c.1761A>C NP_005624.2:p.Ile587=
XM_005264515.3:c.1761A>C XP_005264572.1:p.Ile587=
XM_011533060.1:c.1854A>C XP_011531362.1:p.Ile618=
XM_011533061.1:c.1854A>C XP_011531363.1:p.Ile618=
XM_011533062.1:c.1740A>C XP_011531364.1:p.Ile580=
XM_011533063.1:c.1737A>C XP_011531365.1:p.Ile579=
XM_011533064.1:c.1590A>C XP_011531366.1:p.Ile530=
XM_011533065.1:c.1854A>C XP_011531367.1:p.Ile618=
XM_011533066.1:c.696A>C XP_011531368.1:p.Ile232=
XM_005264515.4:c.1761A>C XP_005264572.1:p.Ile587=
XM_011533062.2:c.1740A>C XP_011531364.1:p.Ile580=
XM_011533064.2:c.1590A>C XP_011531366.1:p.Ile530=
NM_001382394.1:c.1740A>C NP_001369323.1:p.Ile580=
NM_001382395.1:c.1761A>C NP_001369324.1:p.Ile587=
NM_005633.4:c.1761A>C MANE Select NP_005624.2:p.Ile587=
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