Canonical Allele Identifier: CA2136066007

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152963_50152964delinsTC , CM000676.2:g.50152963_50152964delinsTC	GRCh38
NC_000014.8:g.50619681_50619682delinsTC , CM000676.1:g.50619681_50619682delinsTC	GRCh37
NC_000014.7:g.49689431_49689432delinsTC	NCBI36
NG_051073.1:g.83730_83731delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+106_2161+107delinsGA MANE Select	ENSP00000216373.5:n.2161+106_2161+107delinsGA
ENST00000216373.9:c.2161+106_2161+107delinsGA	ENSP00000216373.5:n.2161+106_2161+107delinsGA
ENST00000543680.5:c.2062+106_2062+107delinsGA	ENSP00000445328.1:n.2062+106_2062+107delinsGA
NM_006939.2:c.2161+106_2161+107delinsGA	NP_008870.2:n.2161+106_2161+107delinsGA
XM_005268021.1:c.1981+106_1981+107delinsGA	XP_005268078.1:n.1981+106_1981+107delinsGA
XM_011537103.1:c.2122+106_2122+107delinsGA	XP_011535405.1:n.2122+106_2122+107delinsGA
XM_011537104.1:c.2161+106_2161+107delinsGA	XP_011535406.1:n.2161+106_2161+107delinsGA
NM_006939.3:c.2161+106_2161+107delinsGA	NP_008870.2:n.2161+106_2161+107delinsGA
NM_006939.4:c.2161+106_2161+107delinsGA MANE Select	NP_008870.2:n.2161+106_2161+107delinsGA