Canonical Allele Identifier: CA346372933

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39281769A>T (hg19) ; chr2:g.39054628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054628A>T , CM000664.2:g.39054628A>T	GRCh38
NC_000002.11:g.39281769A>T , CM000664.1:g.39281769A>T	GRCh37
NC_000002.10:g.39135273A>T	NCBI36
NG_007530.1:g.70836T>A , LRG_754:g.70836T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.733T>A
ENST00000685782.1:n.1544T>A
ENST00000688189.1:n.471T>A
ENST00000689668.1:n.713T>A
ENST00000690679.1:c.806T>A
ENST00000690876.1:c.706T>A	ENSP00000508955.1:p.Leu236Met
ENST00000691229.1:c.706T>A	ENSP00000510437.1:p.Leu236Met
ENST00000692089.1:c.706T>A	ENSP00000508626.1:p.Leu236Met
ENST00000402219.8:c.706T>A MANE Select	ENSP00000384675.2:p.Leu236Met
ENST00000395038.6:c.706T>A	ENSP00000378479.2:p.Leu236Met
ENST00000402219.6:c.706T>A	ENSP00000384675.2:p.Leu236Met
ENST00000426016.5:c.706T>A	ENSP00000387784.1:p.Leu236Met
NM_005633.3:c.706T>A , LRG_754t1:c.706T>A	NP_005624.2:p.Leu236Met
XM_005264515.3:c.706T>A	XP_005264572.1:p.Leu236Met
XM_011533060.1:c.799T>A	XP_011531362.1:p.Leu267Met
XM_011533061.1:c.799T>A	XP_011531363.1:p.Leu267Met
XM_011533062.1:c.685T>A	XP_011531364.1:p.Leu229Met
XM_011533063.1:c.682T>A	XP_011531365.1:p.Leu228Met
XM_011533064.1:c.535T>A	XP_011531366.1:p.Leu179Met
XM_011533065.1:c.799T>A	XP_011531367.1:p.Leu267Met
XM_005264515.4:c.706T>A	XP_005264572.1:p.Leu236Met
XM_011533062.2:c.685T>A	XP_011531364.1:p.Leu229Met
XM_011533064.2:c.535T>A	XP_011531366.1:p.Leu179Met
NM_001382394.1:c.685T>A	NP_001369323.1:p.Leu229Met
NM_001382395.1:c.706T>A	NP_001369324.1:p.Leu236Met
NM_005633.4:c.706T>A MANE Select	NP_005624.2:p.Leu236Met