Canonical Allele Identifier: CA346373162
Gene: SOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054731G>C , CM000664.2:g.39054731G>C GRCh38
NC_000002.11:g.39281872G>C , CM000664.1:g.39281872G>C GRCh37
NC_000002.10:g.39135376G>C NCBI36
NG_007530.1:g.70733C>G , LRG_754:g.70733C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.630C>G
ENST00000685782.1:n.1441C>G
ENST00000688189.1:n.368C>G
ENST00000689668.1:n.610C>G
ENST00000690679.1:c.703C>G
ENST00000690876.1:c.603C>G ENSP00000508955.1:p.Tyr201Ter
ENST00000691229.1:c.603C>G ENSP00000510437.1:p.Tyr201Ter
ENST00000692089.1:c.603C>G ENSP00000508626.1:p.Tyr201Ter
ENST00000402219.8:c.603C>G MANE Select ENSP00000384675.2:p.Tyr201Ter
ENST00000395038.6:c.603C>G ENSP00000378479.2:p.Tyr201Ter
ENST00000402219.6:c.603C>G ENSP00000384675.2:p.Tyr201Ter
ENST00000426016.5:c.603C>G ENSP00000387784.1:p.Tyr201Ter
NM_005633.3:c.603C>G , LRG_754t1:c.603C>G NP_005624.2:p.Tyr201Ter
XM_005264515.3:c.603C>G XP_005264572.1:p.Tyr201Ter
XM_011533060.1:c.696C>G XP_011531362.1:p.Tyr232Ter
XM_011533061.1:c.696C>G XP_011531363.1:p.Tyr232Ter
XM_011533062.1:c.582C>G XP_011531364.1:p.Tyr194Ter
XM_011533063.1:c.579C>G XP_011531365.1:p.Tyr193Ter
XM_011533064.1:c.432C>G XP_011531366.1:p.Tyr144Ter
XM_011533065.1:c.696C>G XP_011531367.1:p.Tyr232Ter
XM_005264515.4:c.603C>G XP_005264572.1:p.Tyr201Ter
XM_011533062.2:c.582C>G XP_011531364.1:p.Tyr194Ter
XM_011533064.2:c.432C>G XP_011531366.1:p.Tyr144Ter
NM_001382394.1:c.582C>G NP_001369323.1:p.Tyr194Ter
NM_001382395.1:c.603C>G NP_001369324.1:p.Tyr201Ter
NM_005633.4:c.603C>G MANE Select NP_005624.2:p.Tyr201Ter