Canonical Allele Identifier: CA346365567
Gene: SOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.39249861G>T (hg19) chr2:g.39022720G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022720G>T , CM000664.2:g.39022720G>T GRCh38
NC_000002.11:g.39249861G>T , CM000664.1:g.39249861G>T GRCh37
NC_000002.10:g.39103365G>T NCBI36
NG_007530.1:g.102744C>A , LRG_754:g.102744C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1588C>A
ENST00000685279.1:c.475C>A ENSP00000509424.1:p.Pro159Thr
ENST00000688043.1:n.1929C>A
ENST00000689668.1:n.1715C>A
ENST00000690876.1:c.1597C>A ENSP00000508955.1:p.Pro533Thr
ENST00000691229.1:c.1597C>A ENSP00000510437.1:p.Pro533Thr
ENST00000692089.1:c.1597C>A ENSP00000508626.1:p.Pro533Thr
ENST00000692620.1:c.475C>A ENSP00000509311.1:p.Pro159Thr
ENST00000402219.8:c.1708C>A MANE Select ENSP00000384675.2:p.Pro570Thr
ENST00000395038.6:c.1708C>A ENSP00000378479.2:p.Pro570Thr
ENST00000402219.6:c.1708C>A ENSP00000384675.2:p.Pro570Thr
ENST00000426016.5:c.1708C>A ENSP00000387784.1:p.Pro570Thr
NM_005633.3:c.1708C>A , LRG_754t1:c.1708C>A NP_005624.2:p.Pro570Thr
XM_005264515.3:c.1708C>A XP_005264572.1:p.Pro570Thr
XM_011533060.1:c.1801C>A XP_011531362.1:p.Pro601Thr
XM_011533061.1:c.1801C>A XP_011531363.1:p.Pro601Thr
XM_011533062.1:c.1687C>A XP_011531364.1:p.Pro563Thr
XM_011533063.1:c.1684C>A XP_011531365.1:p.Pro562Thr
XM_011533064.1:c.1537C>A XP_011531366.1:p.Pro513Thr
XM_011533065.1:c.1801C>A XP_011531367.1:p.Pro601Thr
XM_011533066.1:c.643C>A XP_011531368.1:p.Pro215Thr
XM_005264515.4:c.1708C>A XP_005264572.1:p.Pro570Thr
XM_011533062.2:c.1687C>A XP_011531364.1:p.Pro563Thr
XM_011533064.2:c.1537C>A XP_011531366.1:p.Pro513Thr
NM_001382394.1:c.1687C>A NP_001369323.1:p.Pro563Thr
NM_001382395.1:c.1708C>A NP_001369324.1:p.Pro570Thr
NM_005633.4:c.1708C>A MANE Select NP_005624.2:p.Pro570Thr
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