Canonical Allele Identifier: CA2136058812

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130543C= , CM000676.2:g.50130543C=	GRCh38
NC_000014.8:g.50597261C= , CM000676.1:g.50597261C=	GRCh37
NC_000014.7:g.49667011C=	NCBI36
NG_051073.1:g.106151G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3295G= MANE Select	ENSP00000216373.5:p.Asp1099=
ENST00000216373.9:c.3295G=	ENSP00000216373.5:p.Asp1099=
ENST00000543680.5:c.3196G=	ENSP00000445328.1:p.Asp1066=
NM_006939.2:c.3295G=	NP_008870.2:p.Asp1099=
XM_005268021.1:c.3115G=	XP_005268078.1:p.Asp1039=
XM_011537103.1:c.3256G=	XP_011535405.1:p.Asp1086=
NM_006939.3:c.3295G=	NP_008870.2:p.Asp1099=
NM_006939.4:c.3295G= MANE Select	NP_008870.2:p.Asp1099=