Canonical Allele Identifier: CA2136084650

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180631C= , CM000676.2:g.50180631C=	GRCh38
NC_000014.8:g.50647349C= , CM000676.1:g.50647349C=	GRCh37
NC_000014.7:g.49717099C=	NCBI36
NG_051073.1:g.56063G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.910G= MANE Select	ENSP00000216373.5:p.Glu304=
ENST00000216373.9:c.910G=	ENSP00000216373.5:p.Glu304=
ENST00000543680.5:c.910G=	ENSP00000445328.1:p.Glu304=
ENST00000555794.2:c.24G=
NM_006939.2:c.910G=	NP_008870.2:p.Glu304=
XM_005268021.1:c.730G=	XP_005268078.1:p.Glu244=
XM_011537103.1:c.871G=	XP_011535405.1:p.Glu291=
XM_011537104.1:c.910G=	XP_011535406.1:p.Glu304=
XR_943842.1:n.954-3156C=
XR_943843.1:n.954-3156C=
NM_006939.3:c.910G=	NP_008870.2:p.Glu304=
NM_006939.4:c.910G= MANE Select	NP_008870.2:p.Glu304=