Canonical Allele Identifier: CA2136094928

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199850T= , CM000676.2:g.50199850T=	GRCh38
NC_000014.8:g.50666568T= , CM000676.1:g.50666568T=	GRCh37
NC_000014.7:g.49736318T=	NCBI36
NG_051073.1:g.36844A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.351A= MANE Select	ENSP00000216373.5:p.Val117=
ENST00000216373.9:c.351A=	ENSP00000216373.5:p.Val117=
ENST00000543680.5:c.351A=	ENSP00000445328.1:p.Val117=
ENST00000555666.1:n.530A=
ENST00000556469.5:n.322A=
NM_006939.2:c.351A=	NP_008870.2:p.Val117=
XM_005268021.1:c.171A=	XP_005268078.1:p.Val57=
XM_011537103.1:c.312A=	XP_011535405.1:p.Val104=
XM_011537104.1:c.351A=	XP_011535406.1:p.Val117=
XR_943842.1:n.1039+15978T=
XR_943843.1:n.1039+15978T=
NM_006939.3:c.351A=	NP_008870.2:p.Val117=
NM_006939.4:c.351A= MANE Select	NP_008870.2:p.Val117=