Canonical Allele Identifier: CA2136058824

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130575G= , CM000676.2:g.50130575G=	GRCh38
NC_000014.8:g.50597293G= , CM000676.1:g.50597293G=	GRCh37
NC_000014.7:g.49667043G=	NCBI36
NG_051073.1:g.106119C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3263C= MANE Select	ENSP00000216373.5:p.Thr1088=
ENST00000216373.9:c.3263C=	ENSP00000216373.5:p.Thr1088=
ENST00000543680.5:c.3164C=	ENSP00000445328.1:p.Thr1055=
NM_006939.2:c.3263C=	NP_008870.2:p.Thr1088=
XM_005268021.1:c.3083C=	XP_005268078.1:p.Thr1028=
XM_011537103.1:c.3224C=	XP_011535405.1:p.Thr1075=
NM_006939.3:c.3263C=	NP_008870.2:p.Thr1088=
NM_006939.4:c.3263C= MANE Select	NP_008870.2:p.Thr1088=