Canonical Allele Identifier: CA2136058819

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130563G= , CM000676.2:g.50130563G=	GRCh38
NC_000014.8:g.50597281G= , CM000676.1:g.50597281G=	GRCh37
NC_000014.7:g.49667031G=	NCBI36
NG_051073.1:g.106131C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3275C= MANE Select	ENSP00000216373.5:p.Pro1092=
ENST00000216373.9:c.3275C=	ENSP00000216373.5:p.Pro1092=
ENST00000543680.5:c.3176C=	ENSP00000445328.1:p.Pro1059=
NM_006939.2:c.3275C=	NP_008870.2:p.Pro1092=
XM_005268021.1:c.3095C=	XP_005268078.1:p.Pro1032=
XM_011537103.1:c.3236C=	XP_011535405.1:p.Pro1079=
NM_006939.3:c.3275C=	NP_008870.2:p.Pro1092=
NM_006939.4:c.3275C= MANE Select	NP_008870.2:p.Pro1092=