Canonical Allele Identifier: CA2136065861

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152681_50152695delinsATGGTGGCTCATGCC , CM000676.2:g.50152681_50152695delinsATGGTGGCTCATGCC	GRCh38
NC_000014.8:g.50619399_50619413delinsATGGTGGCTCATGCC , CM000676.1:g.50619399_50619413delinsATGGTGGCTCATGCC	GRCh37
NC_000014.7:g.49689149_49689163delinsATGGTGGCTCATGCC	NCBI36
NG_051073.1:g.83999_84013delinsGGCATGAGCCACCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+375_2161+389delinsGGCATGAGCCACCAT MANE Select	ENSP00000216373.5:n.2161+375_2161+389delinsGGCATGAGCCACCAT
ENST00000216373.9:c.2161+375_2161+389delinsGGCATGAGCCACCAT	ENSP00000216373.5:n.2161+375_2161+389delinsGGCATGAGCCACCAT
ENST00000543680.5:c.2062+375_2062+389delinsGGCATGAGCCACCAT	ENSP00000445328.1:n.2062+375_2062+389delinsGGCATGAGCCACCAT
NM_006939.2:c.2161+375_2161+389delinsGGCATGAGCCACCAT	NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT
XM_005268021.1:c.1981+375_1981+389delinsGGCATGAGCCACCAT	XP_005268078.1:n.1981+375_1981+389delinsGGCATGAGCCACCAT
XM_011537103.1:c.2122+375_2122+389delinsGGCATGAGCCACCAT	XP_011535405.1:n.2122+375_2122+389delinsGGCATGAGCCACCAT
XM_011537104.1:c.2161+375_2161+389delinsGGCATGAGCCACCAT	XP_011535406.1:n.2161+375_2161+389delinsGGCATGAGCCACCAT
NM_006939.3:c.2161+375_2161+389delinsGGCATGAGCCACCAT	NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT
NM_006939.4:c.2161+375_2161+389delinsGGCATGAGCCACCAT MANE Select	NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT