Canonical Allele Identifier: CA7177172

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50156983_50156984del , CM000676.2:g.50156983_50156984del	GRCh38
NC_000014.8:g.50623701_50623702del , CM000676.1:g.50623701_50623702del	GRCh37
NC_000014.7:g.49693451_49693452del	NCBI36
NG_051073.1:g.79714_79715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2057+19_2057+20del MANE Select	ENSP00000216373.5:n.2057+19_2057+20del
ENST00000216373.9:c.2057+19_2057+20del	ENSP00000216373.5:n.2057+19_2057+20del
ENST00000543680.5:c.1958+19_1958+20del	ENSP00000445328.1:n.1958+19_1958+20del
ENST00000555794.2:c.1190_1191del
NM_006939.2:c.2057+19_2057+20del	NP_008870.2:n.2057+19_2057+20del
XM_005268021.1:c.1877+19_1877+20del	XP_005268078.1:n.1877+19_1877+20del
XM_011537103.1:c.2018+19_2018+20del	XP_011535405.1:n.2018+19_2018+20del
XM_011537104.1:c.2057+19_2057+20del	XP_011535406.1:n.2057+19_2057+20del
NM_006939.3:c.2057+19_2057+20del	NP_008870.2:n.2057+19_2057+20del
NM_006939.4:c.2057+19_2057+20del MANE Select	NP_008870.2:n.2057+19_2057+20del