Canonical Allele Identifier: CA10615218

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38985128C>T , CM000664.2:g.38985128C>T	GRCh38
NC_000002.11:g.39212269C>T , CM000664.1:g.39212269C>T	GRCh37
NC_000002.10:g.39065773C>T	NCBI36
NG_007530.1:g.140336G>A , LRG_754:g.140336G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005633.4:c.*696G>A MANE Select	NP_005624.2:n.*696G>A
ENST00000402219.8:c.*696G>A MANE Select	ENSP00000384675.2:n.*696G>A
NM_001382394.1:c.*696G>A	NP_001369323.1:n.*696G>A
NM_001382395.1:c.*696G>A	NP_001369324.1:n.*696G>A
NM_005633.3:c.*696G>A , LRG_754t1:c.*696G>A	NP_005624.2:n.*696G>A
ENST00000402219.6:c.*696G>A	ENSP00000384675.2:n.*696G>A
ENST00000426016.5:c.*696G>A	ENSP00000387784.1:n.*696G>A
ENST00000685279.1:c.*696G>A	ENSP00000509424.1:n.*696G>A
ENST00000686849.1:n.1489G>A
ENST00000690876.1:c.*2004G>A	ENSP00000508955.1:n.*2004G>A
ENST00000692089.1:c.3399+2345G>A	ENSP00000508626.1:n.3399+2345G>A
ENST00000692227.1:c.1397G>A	ENSP00000509138.1:n.1397G>A
XM_005264515.3:c.*696G>A	XP_005264572.1:n.*696G>A
XM_005264515.4:c.*696G>A	XP_005264572.1:n.*696G>A
XM_011533060.1:c.*696G>A	XP_011531362.1:n.*696G>A
XM_011533061.1:c.*696G>A	XP_011531363.1:n.*696G>A
XM_011533062.1:c.*696G>A	XP_011531364.1:n.*696G>A
XM_011533062.2:c.*696G>A	XP_011531364.1:n.*696G>A
XM_011533063.1:c.*696G>A	XP_011531365.1:n.*696G>A
XM_011533064.1:c.*696G>A	XP_011531366.1:n.*696G>A
XM_011533064.2:c.*696G>A	XP_011531366.1:n.*696G>A
XM_011533065.1:c.*182G>A	XP_011531367.1:n.*182G>A
XM_011533066.1:c.*696G>A	XP_011531368.1:n.*696G>A