Canonical Allele Identifier: CA2136094903

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199779A= , CM000676.2:g.50199779A=	GRCh38
NC_000014.8:g.50666497A= , CM000676.1:g.50666497A=	GRCh37
NC_000014.7:g.49736247A=	NCBI36
NG_051073.1:g.36915T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.422T= MANE Select	ENSP00000216373.5:p.Ile141=
ENST00000216373.9:c.422T=	ENSP00000216373.5:p.Ile141=
ENST00000543680.5:c.422T=	ENSP00000445328.1:p.Ile141=
ENST00000555666.1:n.601T=
ENST00000556469.5:n.393T=
NM_006939.2:c.422T=	NP_008870.2:p.Ile141=
XM_005268021.1:c.242T=	XP_005268078.1:p.Ile81=
XM_011537103.1:c.383T=	XP_011535405.1:p.Ile128=
XM_011537104.1:c.422T=	XP_011535406.1:p.Ile141=
XR_943842.1:n.1039+15907A=
XR_943843.1:n.1039+15907A=
NM_006939.3:c.422T=	NP_008870.2:p.Ile141=
NM_006939.4:c.422T= MANE Select	NP_008870.2:p.Ile141=