Canonical Allele Identifier: CA2136058820

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130566G= , CM000676.2:g.50130566G=	GRCh38
NC_000014.8:g.50597284G= , CM000676.1:g.50597284G=	GRCh37
NC_000014.7:g.49667034G=	NCBI36
NG_051073.1:g.106128C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3272C= MANE Select	ENSP00000216373.5:p.Thr1091=
ENST00000216373.9:c.3272C=	ENSP00000216373.5:p.Thr1091=
ENST00000543680.5:c.3173C=	ENSP00000445328.1:p.Thr1058=
NM_006939.2:c.3272C=	NP_008870.2:p.Thr1091=
XM_005268021.1:c.3092C=	XP_005268078.1:p.Thr1031=
XM_011537103.1:c.3233C=	XP_011535405.1:p.Thr1078=
NM_006939.3:c.3272C=	NP_008870.2:p.Thr1091=
NM_006939.4:c.3272C= MANE Select	NP_008870.2:p.Thr1091=