Canonical Allele Identifier: CA1139656895

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38982931G>T , CM000664.2:g.38982931G>T	GRCh38
NC_000002.11:g.39210072G>T , CM000664.1:g.39210072G>T	GRCh37
NC_000002.10:g.39063576G>T	NCBI36
NG_007530.1:g.142533C>A , LRG_754:g.142533C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.*2893C>A	ENSP00000509424.1:n.*2893C>A
ENST00000692089.1:c.3399+4542C>A	ENSP00000508626.1:n.3399+4542C>A
ENST00000402219.8:c.*2893C>A MANE Select	ENSP00000384675.2:n.*2893C>A
ENST00000402219.6:c.*2893C>A	ENSP00000384675.2:n.*2893C>A
ENST00000426016.5:c.*2893C>A	ENSP00000387784.1:n.*2893C>A
NM_005633.3:c.*2893C>A , LRG_754t1:c.*2893C>A	NP_005624.2:n.*2893C>A
XM_005264515.3:c.*2893C>A	XP_005264572.1:n.*2893C>A
XM_011533060.1:c.*2893C>A	XP_011531362.1:n.*2893C>A
XM_011533061.1:c.*2893C>A	XP_011531363.1:n.*2893C>A
XM_011533062.1:c.*2893C>A	XP_011531364.1:n.*2893C>A
XM_011533063.1:c.*2893C>A	XP_011531365.1:n.*2893C>A
XM_011533064.1:c.*2893C>A	XP_011531366.1:n.*2893C>A
XM_011533065.1:c.*2379C>A	XP_011531367.1:n.*2379C>A
XM_011533066.1:c.*2893C>A	XP_011531368.1:n.*2893C>A
XM_005264515.4:c.*2893C>A	XP_005264572.1:n.*2893C>A
NM_001382394.1:c.*2893C>A	NP_001369323.1:n.*2893C>A
NM_001382395.1:c.*2893C>A	NP_001369324.1:n.*2893C>A
NM_005633.4:c.*2893C>A MANE Select	NP_005624.2:n.*2893C>A