Canonical Allele Identifier: CA2136039754

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150226T= , CM000676.2:g.50150226T=	GRCh38
NC_000014.8:g.50616944T= , CM000676.1:g.50616944T=	GRCh37
NC_000014.7:g.49686694T=	NCBI36
NG_051073.1:g.86468A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2166A= MANE Select	ENSP00000216373.5:p.Lys722=
ENST00000216373.9:c.2166A=	ENSP00000216373.5:p.Lys722=
ENST00000543680.5:c.2067A=	ENSP00000445328.1:p.Lys689=
NM_006939.2:c.2166A=	NP_008870.2:p.Lys722=
XM_005268021.1:c.1986A=	XP_005268078.1:p.Lys662=
XM_011537103.1:c.2127A=	XP_011535405.1:p.Lys709=
XM_011537104.1:c.2166A=	XP_011535406.1:p.Lys722=
NM_006939.3:c.2166A=	NP_008870.2:p.Lys722=
NM_006939.4:c.2166A= MANE Select	NP_008870.2:p.Lys722=