Canonical Allele Identifier: CA425866430

Gene: SOS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38985995T>C , CM000664.2:g.38985995T>C	GRCh38
NC_000002.11:g.39213136T>C , CM000664.1:g.39213136T>C	GRCh37
NC_000002.10:g.39066640T>C	NCBI36
NG_007530.1:g.139469A>G , LRG_754:g.139469A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.2598A>G	ENSP00000509424.1:p.Pro866=
ENST00000686849.1:n.622A>G
ENST00000690876.1:c.*1137A>G	ENSP00000508955.1:n.*1137A>G
ENST00000692089.1:c.3399+1478A>G	ENSP00000508626.1:n.3399+1478A>G
ENST00000692227.1:c.1162-632A>G	ENSP00000509138.1:n.1162-632A>G
ENST00000402219.8:c.3831A>G MANE Select	ENSP00000384675.2:p.Pro1277=
ENST00000395038.6:c.3786A>G	ENSP00000378479.2:p.Pro1262=
ENST00000402219.6:c.3831A>G	ENSP00000384675.2:p.Pro1277=
ENST00000426016.5:c.3831A>G	ENSP00000387784.1:p.Pro1277=
NM_005633.3:c.3831A>G , LRG_754t1:c.3831A>G	NP_005624.2:p.Pro1277=
XM_005264515.3:c.3786A>G	XP_005264572.1:p.Pro1262=
XM_011533060.1:c.3924A>G	XP_011531362.1:p.Pro1308=
XM_011533061.1:c.3879A>G	XP_011531363.1:p.Pro1293=
XM_011533062.1:c.3810A>G	XP_011531364.1:p.Pro1270=
XM_011533063.1:c.3807A>G	XP_011531365.1:p.Pro1269=
XM_011533064.1:c.3660A>G	XP_011531366.1:p.Pro1220=
XM_011533065.1:c.3604-632A>G	XP_011531367.1:n.3604-632A>G
XM_011533066.1:c.2766A>G	XP_011531368.1:p.Pro922=
XM_005264515.4:c.3786A>G	XP_005264572.1:p.Pro1262=
XM_011533062.2:c.3810A>G	XP_011531364.1:p.Pro1270=
XM_011533064.2:c.3660A>G	XP_011531366.1:p.Pro1220=
NM_001382394.1:c.3810A>G	NP_001369323.1:p.Pro1270=
NM_001382395.1:c.3786A>G	NP_001369324.1:p.Pro1262=
NM_005633.4:c.3831A>G MANE Select	NP_005624.2:p.Pro1277=