Canonical Allele Identifier: CA2136058826

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130578T= , CM000676.2:g.50130578T=	GRCh38
NC_000014.8:g.50597296T= , CM000676.1:g.50597296T=	GRCh37
NC_000014.7:g.49667046T=	NCBI36
NG_051073.1:g.106116A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3260A= MANE Select	ENSP00000216373.5:p.Asn1087=
ENST00000216373.9:c.3260A=	ENSP00000216373.5:p.Asn1087=
ENST00000543680.5:c.3161A=	ENSP00000445328.1:p.Asn1054=
NM_006939.2:c.3260A=	NP_008870.2:p.Asn1087=
XM_005268021.1:c.3080A=	XP_005268078.1:p.Asn1027=
XM_011537103.1:c.3221A=	XP_011535405.1:p.Asn1074=
NM_006939.3:c.3260A=	NP_008870.2:p.Asn1087=
NM_006939.4:c.3260A= MANE Select	NP_008870.2:p.Asn1087=