Canonical Allele Identifier: CA2136094924

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199839T= , CM000676.2:g.50199839T=	GRCh38
NC_000014.8:g.50666557T= , CM000676.1:g.50666557T=	GRCh37
NC_000014.7:g.49736307T=	NCBI36
NG_051073.1:g.36855A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.362A= MANE Select	ENSP00000216373.5:p.Lys121=
ENST00000216373.9:c.362A=	ENSP00000216373.5:p.Lys121=
ENST00000543680.5:c.362A=	ENSP00000445328.1:p.Lys121=
ENST00000555666.1:n.541A=
ENST00000556469.5:n.333A=
NM_006939.2:c.362A=	NP_008870.2:p.Lys121=
XM_005268021.1:c.182A=	XP_005268078.1:p.Lys61=
XM_011537103.1:c.323A=	XP_011535405.1:p.Lys108=
XM_011537104.1:c.362A=	XP_011535406.1:p.Lys121=
XR_943842.1:n.1039+15967T=
XR_943843.1:n.1039+15967T=
NM_006939.3:c.362A=	NP_008870.2:p.Lys121=
NM_006939.4:c.362A= MANE Select	NP_008870.2:p.Lys121=