Canonical Allele Identifier: CA2136058797

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130512T= , CM000676.2:g.50130512T=	GRCh38
NC_000014.8:g.50597230T= , CM000676.1:g.50597230T=	GRCh37
NC_000014.7:g.49666980T=	NCBI36
NG_051073.1:g.106182A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3326A= MANE Select	ENSP00000216373.5:p.Asn1109=
ENST00000216373.9:c.3326A=	ENSP00000216373.5:p.Asn1109=
ENST00000543680.5:c.3227A=	ENSP00000445328.1:p.Asn1076=
NM_006939.2:c.3326A=	NP_008870.2:p.Asn1109=
XM_005268021.1:c.3146A=	XP_005268078.1:p.Asn1049=
XM_011537103.1:c.3287A=	XP_011535405.1:p.Asn1096=
NM_006939.3:c.3326A=	NP_008870.2:p.Asn1109=
NM_006939.4:c.3326A= MANE Select	NP_008870.2:p.Asn1109=