Canonical Allele Identifier: CA346373119
Gene: SOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054712A>G , CM000664.2:g.39054712A>G GRCh38
NC_000002.11:g.39281853A>G , CM000664.1:g.39281853A>G GRCh37
NC_000002.10:g.39135357A>G NCBI36
NG_007530.1:g.70752T>C , LRG_754:g.70752T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461545.2:n.649T>C
ENST00000685782.1:n.1460T>C
ENST00000688189.1:n.387T>C
ENST00000689668.1:n.629T>C
ENST00000690679.1:c.722T>C
ENST00000690876.1:c.622T>C ENSP00000508955.1:p.Phe208Leu
ENST00000691229.1:c.622T>C ENSP00000510437.1:p.Phe208Leu
ENST00000692089.1:c.622T>C ENSP00000508626.1:p.Phe208Leu
ENST00000402219.8:c.622T>C MANE Select ENSP00000384675.2:p.Phe208Leu
ENST00000395038.6:c.622T>C ENSP00000378479.2:p.Phe208Leu
ENST00000402219.6:c.622T>C ENSP00000384675.2:p.Phe208Leu
ENST00000426016.5:c.622T>C ENSP00000387784.1:p.Phe208Leu
NM_005633.3:c.622T>C , LRG_754t1:c.622T>C NP_005624.2:p.Phe208Leu
XM_005264515.3:c.622T>C XP_005264572.1:p.Phe208Leu
XM_011533060.1:c.715T>C XP_011531362.1:p.Phe239Leu
XM_011533061.1:c.715T>C XP_011531363.1:p.Phe239Leu
XM_011533062.1:c.601T>C XP_011531364.1:p.Phe201Leu
XM_011533063.1:c.598T>C XP_011531365.1:p.Phe200Leu
XM_011533064.1:c.451T>C XP_011531366.1:p.Phe151Leu
XM_011533065.1:c.715T>C XP_011531367.1:p.Phe239Leu
XM_005264515.4:c.622T>C XP_005264572.1:p.Phe208Leu
XM_011533062.2:c.601T>C XP_011531364.1:p.Phe201Leu
XM_011533064.2:c.451T>C XP_011531366.1:p.Phe151Leu
NM_001382394.1:c.601T>C NP_001369323.1:p.Phe201Leu
NM_001382395.1:c.622T>C NP_001369324.1:p.Phe208Leu
NM_005633.4:c.622T>C MANE Select NP_005624.2:p.Phe208Leu