Canonical Allele Identifier: CA2698906981

Gene: SOS1

Linked Data

• dbSNP Id: rs2124450673

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38984425A>C , CM000664.2:g.38984425A>C	GRCh38
NC_000002.11:g.39211566A>C , CM000664.1:g.39211566A>C	GRCh37
NC_000002.10:g.39065070A>C	NCBI36
NG_007530.1:g.141039T>G , LRG_754:g.141039T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.*1399T>G	ENSP00000509424.1:n.*1399T>G
ENST00000686849.1:n.2192T>G
ENST00000690876.1:c.*2707T>G	ENSP00000508955.1:n.*2707T>G
ENST00000692089.1:c.3399+3048T>G	ENSP00000508626.1:n.3399+3048T>G
ENST00000402219.8:c.*1399T>G MANE Select	ENSP00000384675.2:n.*1399T>G
ENST00000402219.6:c.*1399T>G	ENSP00000384675.2:n.*1399T>G
ENST00000426016.5:c.*1399T>G	ENSP00000387784.1:n.*1399T>G
NM_005633.3:c.*1399T>G , LRG_754t1:c.*1399T>G	NP_005624.2:n.*1399T>G
XM_005264515.3:c.*1399T>G	XP_005264572.1:n.*1399T>G
XM_011533060.1:c.*1399T>G	XP_011531362.1:n.*1399T>G
XM_011533061.1:c.*1399T>G	XP_011531363.1:n.*1399T>G
XM_011533062.1:c.*1399T>G	XP_011531364.1:n.*1399T>G
XM_011533063.1:c.*1399T>G	XP_011531365.1:n.*1399T>G
XM_011533064.1:c.*1399T>G	XP_011531366.1:n.*1399T>G
XM_011533065.1:c.*885T>G	XP_011531367.1:n.*885T>G
XM_011533066.1:c.*1399T>G	XP_011531368.1:n.*1399T>G
XM_005264515.4:c.*1399T>G	XP_005264572.1:n.*1399T>G
XM_011533062.2:c.*1399T>G	XP_011531364.1:n.*1399T>G
XM_011533064.2:c.*1399T>G	XP_011531366.1:n.*1399T>G
NM_001382394.1:c.*1399T>G	NP_001369323.1:n.*1399T>G
NM_001382395.1:c.*1399T>G	NP_001369324.1:n.*1399T>G
NM_005633.4:c.*1399T>G MANE Select	NP_005624.2:n.*1399T>G