Canonical Allele Identifier: CA45675737

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39024153G>A , CM000664.2:g.39024153G>A	GRCh38
NC_000002.11:g.39251294G>A , CM000664.1:g.39251294G>A	GRCh37
NC_000002.10:g.39104798G>A	NCBI36
NG_007530.1:g.101311C>T , LRG_754:g.101311C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005633.4:c.1075-16C>T MANE Select	NP_005624.2:n.1075-16C>T
ENST00000402219.8:c.1075-16C>T MANE Select	ENSP00000384675.2:n.1075-16C>T
NM_001382394.1:c.1054-16C>T	NP_001369323.1:n.1054-16C>T
NM_001382395.1:c.1075-16C>T	NP_001369324.1:n.1075-16C>T
NM_005633.3:c.1075-16C>T , LRG_754t1:c.1075-16C>T	NP_005624.2:n.1075-16C>T
ENST00000395038.6:c.1075-16C>T	ENSP00000378479.2:n.1075-16C>T
ENST00000402219.6:c.1075-16C>T	ENSP00000384675.2:n.1075-16C>T
ENST00000426016.5:c.1075-16C>T	ENSP00000387784.1:n.1075-16C>T
ENST00000461545.1:n.425-16C>T
ENST00000472480.2:n.955-16C>T
ENST00000688043.1:n.1280C>T
ENST00000689668.1:n.1082-16C>T
ENST00000690679.1:c.1262-16C>T
ENST00000690876.1:c.964-16C>T	ENSP00000508955.1:n.964-16C>T
ENST00000691229.1:c.964-16C>T	ENSP00000510437.1:n.964-16C>T
ENST00000692089.1:c.964-16C>T	ENSP00000508626.1:n.964-16C>T
XM_005264515.3:c.1075-16C>T	XP_005264572.1:n.1075-16C>T
XM_005264515.4:c.1075-16C>T	XP_005264572.1:n.1075-16C>T
XM_011533060.1:c.1168-16C>T	XP_011531362.1:n.1168-16C>T
XM_011533061.1:c.1168-16C>T	XP_011531363.1:n.1168-16C>T
XM_011533062.1:c.1054-16C>T	XP_011531364.1:n.1054-16C>T
XM_011533062.2:c.1054-16C>T	XP_011531364.1:n.1054-16C>T
XM_011533063.1:c.1051-16C>T	XP_011531365.1:n.1051-16C>T
XM_011533064.1:c.904-16C>T	XP_011531366.1:n.904-16C>T
XM_011533064.2:c.904-16C>T	XP_011531366.1:n.904-16C>T
XM_011533065.1:c.1168-16C>T	XP_011531367.1:n.1168-16C>T
XM_011533066.1:c.10-16C>T	XP_011531368.1:n.10-16C>T