Canonical Allele Identifier: CA346364240

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39239382G>C (hg19) ; chr2:g.39012241G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39012241G>C , CM000664.2:g.39012241G>C	GRCh38
NC_000002.11:g.39239382G>C , CM000664.1:g.39239382G>C	GRCh37
NC_000002.10:g.39092886G>C	NCBI36
NG_007530.1:g.113223C>G , LRG_754:g.113223C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.1042C>G	ENSP00000509424.1:p.Pro348Ala
ENST00000688043.1:n.3607C>G
ENST00000689668.1:n.2282C>G
ENST00000690514.1:n.364C>G
ENST00000690876.1:c.2164C>G	ENSP00000508955.1:p.Pro722Ala
ENST00000691229.1:c.2164C>G	ENSP00000510437.1:p.Pro722Ala
ENST00000692089.1:c.2164C>G	ENSP00000508626.1:p.Pro722Ala
ENST00000692620.1:c.934+1219C>G	ENSP00000509311.1:n.934+1219C>G
ENST00000402219.8:c.2275C>G MANE Select	ENSP00000384675.2:p.Pro759Ala
ENST00000395038.6:c.2275C>G	ENSP00000378479.2:p.Pro759Ala
ENST00000402219.6:c.2275C>G	ENSP00000384675.2:p.Pro759Ala
ENST00000426016.5:c.2275C>G	ENSP00000387784.1:p.Pro759Ala
NM_005633.3:c.2275C>G , LRG_754t1:c.2275C>G	NP_005624.2:p.Pro759Ala
XM_005264515.3:c.2275C>G	XP_005264572.1:p.Pro759Ala
XM_011533060.1:c.2368C>G	XP_011531362.1:p.Pro790Ala
XM_011533061.1:c.2368C>G	XP_011531363.1:p.Pro790Ala
XM_011533062.1:c.2254C>G	XP_011531364.1:p.Pro752Ala
XM_011533063.1:c.2251C>G	XP_011531365.1:p.Pro751Ala
XM_011533064.1:c.2104C>G	XP_011531366.1:p.Pro702Ala
XM_011533065.1:c.2368C>G	XP_011531367.1:p.Pro790Ala
XM_011533066.1:c.1210C>G	XP_011531368.1:p.Pro404Ala
XM_005264515.4:c.2275C>G	XP_005264572.1:p.Pro759Ala
XM_011533062.2:c.2254C>G	XP_011531364.1:p.Pro752Ala
XM_011533064.2:c.2104C>G	XP_011531366.1:p.Pro702Ala
NM_001382394.1:c.2254C>G	NP_001369323.1:p.Pro752Ala
NM_001382395.1:c.2275C>G	NP_001369324.1:p.Pro759Ala
NM_005633.4:c.2275C>G MANE Select	NP_005624.2:p.Pro759Ala