Canonical Allele Identifier: CA2136094896

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199752A= , CM000676.2:g.50199752A=	GRCh38
NC_000014.8:g.50666470A= , CM000676.1:g.50666470A=	GRCh37
NC_000014.7:g.49736220A=	NCBI36
NG_051073.1:g.36942T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.449T= MANE Select	ENSP00000216373.5:p.Phe150=
ENST00000216373.9:c.449T=	ENSP00000216373.5:p.Phe150=
ENST00000543680.5:c.449T=	ENSP00000445328.1:p.Phe150=
ENST00000555666.1:n.628T=
ENST00000556469.5:n.420T=
NM_006939.2:c.449T=	NP_008870.2:p.Phe150=
XM_005268021.1:c.269T=	XP_005268078.1:p.Phe90=
XM_011537103.1:c.410T=	XP_011535405.1:p.Phe137=
XM_011537104.1:c.449T=	XP_011535406.1:p.Phe150=
XR_943842.1:n.1039+15880A=
XR_943843.1:n.1039+15880A=
NM_006939.3:c.449T=	NP_008870.2:p.Phe150=
NM_006939.4:c.449T= MANE Select	NP_008870.2:p.Phe150=