Canonical Allele Identifier: CA346366184
Gene: SOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.39250137G>T (hg19) chr2:g.39022996G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39022996G>T , CM000664.2:g.39022996G>T GRCh38
NC_000002.11:g.39250137G>T , CM000664.1:g.39250137G>T GRCh37
NC_000002.10:g.39103641G>T NCBI36
NG_007530.1:g.102468C>A , LRG_754:g.102468C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000472480.2:n.1312C>A
ENST00000685279.1:c.199C>A ENSP00000509424.1:p.Pro67Thr
ENST00000688043.1:n.1653C>A
ENST00000689668.1:n.1439C>A
ENST00000690876.1:c.1321C>A ENSP00000508955.1:p.Pro441Thr
ENST00000691229.1:c.1321C>A ENSP00000510437.1:p.Pro441Thr
ENST00000692089.1:c.1321C>A ENSP00000508626.1:p.Pro441Thr
ENST00000692620.1:c.199C>A ENSP00000509311.1:p.Pro67Thr
ENST00000402219.8:c.1432C>A MANE Select ENSP00000384675.2:p.Pro478Thr
ENST00000395038.6:c.1432C>A ENSP00000378479.2:p.Pro478Thr
ENST00000402219.6:c.1432C>A ENSP00000384675.2:p.Pro478Thr
ENST00000426016.5:c.1432C>A ENSP00000387784.1:p.Pro478Thr
ENST00000472480.1:n.276C>A
NM_005633.3:c.1432C>A , LRG_754t1:c.1432C>A NP_005624.2:p.Pro478Thr
XM_005264515.3:c.1432C>A XP_005264572.1:p.Pro478Thr
XM_011533060.1:c.1525C>A XP_011531362.1:p.Pro509Thr
XM_011533061.1:c.1525C>A XP_011531363.1:p.Pro509Thr
XM_011533062.1:c.1411C>A XP_011531364.1:p.Pro471Thr
XM_011533063.1:c.1408C>A XP_011531365.1:p.Pro470Thr
XM_011533064.1:c.1261C>A XP_011531366.1:p.Pro421Thr
XM_011533065.1:c.1525C>A XP_011531367.1:p.Pro509Thr
XM_011533066.1:c.367C>A XP_011531368.1:p.Pro123Thr
XM_005264515.4:c.1432C>A XP_005264572.1:p.Pro478Thr
XM_011533062.2:c.1411C>A XP_011531364.1:p.Pro471Thr
XM_011533064.2:c.1261C>A XP_011531366.1:p.Pro421Thr
NM_001382394.1:c.1411C>A NP_001369323.1:p.Pro471Thr
NM_001382395.1:c.1432C>A NP_001369324.1:p.Pro478Thr
NM_005633.4:c.1432C>A MANE Select NP_005624.2:p.Pro478Thr
Search 100 bp 5'
Search 100 bp 3'