Canonical Allele Identifier: CA1246140918

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39024080T= , CM000664.2:g.39024080T=	GRCh38
NC_000002.11:g.39251221T= , CM000664.1:g.39251221T=	GRCh37
NC_000002.10:g.39104725T=	NCBI36
NG_007530.1:g.101384A= , LRG_754:g.101384A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005633.4:c.1132A= MANE Select	NP_005624.2:p.Thr378=
ENST00000402219.8:c.1132A= MANE Select	ENSP00000384675.2:p.Thr378=
NM_001382394.1:c.1111A=	NP_001369323.1:p.Thr371=
NM_001382395.1:c.1132A=	NP_001369324.1:p.Thr378=
NM_005633.3:c.1132A= , LRG_754t1:c.1132A=	NP_005624.2:p.Thr378=
ENST00000395038.6:c.1132A=	ENSP00000378479.2:p.Thr378=
ENST00000402219.6:c.1132A=	ENSP00000384675.2:p.Thr378=
ENST00000426016.5:c.1132A=	ENSP00000387784.1:p.Thr378=
ENST00000472480.2:n.1012A=
ENST00000688043.1:n.1353A=
ENST00000689668.1:n.1139A=
ENST00000690679.1:c.1319A=
ENST00000690876.1:c.1021A=	ENSP00000508955.1:p.Thr341=
ENST00000691229.1:c.1021A=	ENSP00000510437.1:p.Thr341=
ENST00000692089.1:c.1021A=	ENSP00000508626.1:p.Thr341=
XM_005264515.3:c.1132A=	XP_005264572.1:p.Thr378=
XM_005264515.4:c.1132A=	XP_005264572.1:p.Thr378=
XM_011533060.1:c.1225A=	XP_011531362.1:p.Thr409=
XM_011533061.1:c.1225A=	XP_011531363.1:p.Thr409=
XM_011533062.1:c.1111A=	XP_011531364.1:p.Thr371=
XM_011533062.2:c.1111A=	XP_011531364.1:p.Thr371=
XM_011533063.1:c.1108A=	XP_011531365.1:p.Thr370=
XM_011533064.1:c.961A=	XP_011531366.1:p.Thr321=
XM_011533064.2:c.961A=	XP_011531366.1:p.Thr321=
XM_011533065.1:c.1225A=	XP_011531367.1:p.Thr409=
XM_011533066.1:c.67A=	XP_011531368.1:p.Thr23=