Canonical Allele Identifier: CA2136065862

Gene: SOS2

Linked Data

• dbSNP Id: rs1884697698

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152684_50152697del , CM000676.2:g.50152684_50152697del	GRCh38
NC_000014.8:g.50619402_50619415del , CM000676.1:g.50619402_50619415del	GRCh37
NC_000014.7:g.49689152_49689165del	NCBI36
NG_051073.1:g.83999_84012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+375_2161+388del MANE Select	ENSP00000216373.5:n.2161+375_2161+388del
ENST00000216373.9:c.2161+375_2161+388del	ENSP00000216373.5:n.2161+375_2161+388del
ENST00000543680.5:c.2062+375_2062+388del	ENSP00000445328.1:n.2062+375_2062+388del
NM_006939.2:c.2161+375_2161+388del	NP_008870.2:n.2161+375_2161+388del
XM_005268021.1:c.1981+375_1981+388del	XP_005268078.1:n.1981+375_1981+388del
XM_011537103.1:c.2122+375_2122+388del	XP_011535405.1:n.2122+375_2122+388del
XM_011537104.1:c.2161+375_2161+388del	XP_011535406.1:n.2161+375_2161+388del
NM_006939.3:c.2161+375_2161+388del	NP_008870.2:n.2161+375_2161+388del
NM_006939.4:c.2161+375_2161+388del MANE Select	NP_008870.2:n.2161+375_2161+388del