Canonical Allele Identifier: CA346366450

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023112T>A , CM000664.2:g.39023112T>A	GRCh38
NC_000002.11:g.39250253T>A , CM000664.1:g.39250253T>A	GRCh37
NC_000002.10:g.39103757T>A	NCBI36
NG_007530.1:g.102352A>T , LRG_754:g.102352A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1196A>T
ENST00000685279.1:c.83A>T	ENSP00000509424.1:p.Gln28Leu
ENST00000688043.1:n.1537A>T
ENST00000689668.1:n.1323A>T
ENST00000690876.1:c.1205A>T	ENSP00000508955.1:p.Gln402Leu
ENST00000691229.1:c.1205A>T	ENSP00000510437.1:p.Gln402Leu
ENST00000692089.1:c.1205A>T	ENSP00000508626.1:p.Gln402Leu
ENST00000692620.1:c.83A>T	ENSP00000509311.1:p.Gln28Leu
ENST00000402219.8:c.1316A>T MANE Select	ENSP00000384675.2:p.Gln439Leu
ENST00000395038.6:c.1316A>T	ENSP00000378479.2:p.Gln439Leu
ENST00000402219.6:c.1316A>T	ENSP00000384675.2:p.Gln439Leu
ENST00000426016.5:c.1316A>T	ENSP00000387784.1:p.Gln439Leu
ENST00000472480.1:n.160A>T
NM_005633.3:c.1316A>T , LRG_754t1:c.1316A>T	NP_005624.2:p.Gln439Leu
XM_005264515.3:c.1316A>T	XP_005264572.1:p.Gln439Leu
XM_011533060.1:c.1409A>T	XP_011531362.1:p.Gln470Leu
XM_011533061.1:c.1409A>T	XP_011531363.1:p.Gln470Leu
XM_011533062.1:c.1295A>T	XP_011531364.1:p.Gln432Leu
XM_011533063.1:c.1292A>T	XP_011531365.1:p.Gln431Leu
XM_011533064.1:c.1145A>T	XP_011531366.1:p.Gln382Leu
XM_011533065.1:c.1409A>T	XP_011531367.1:p.Gln470Leu
XM_011533066.1:c.251A>T	XP_011531368.1:p.Gln84Leu
XM_005264515.4:c.1316A>T	XP_005264572.1:p.Gln439Leu
XM_011533062.2:c.1295A>T	XP_011531364.1:p.Gln432Leu
XM_011533064.2:c.1145A>T	XP_011531366.1:p.Gln382Leu
NM_001382394.1:c.1295A>T	NP_001369323.1:p.Gln432Leu
NM_001382395.1:c.1316A>T	NP_001369324.1:p.Gln439Leu
NM_005633.4:c.1316A>T MANE Select	NP_005624.2:p.Gln439Leu