Canonical Allele Identifier: CA2801534058

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152977_50152981del , CM000676.2:g.50152977_50152981del	GRCh38
NC_000014.8:g.50619695_50619699del , CM000676.1:g.50619695_50619699del	GRCh37
NC_000014.7:g.49689445_49689449del	NCBI36
NG_051073.1:g.83713_83717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+89_2161+93del MANE Select	ENSP00000216373.5:n.2161+89_2161+93del
ENST00000216373.9:c.2161+89_2161+93del	ENSP00000216373.5:n.2161+89_2161+93del
ENST00000543680.5:c.2062+89_2062+93del	ENSP00000445328.1:n.2062+89_2062+93del
NM_006939.2:c.2161+89_2161+93del	NP_008870.2:n.2161+89_2161+93del
XM_005268021.1:c.1981+89_1981+93del	XP_005268078.1:n.1981+89_1981+93del
XM_011537103.1:c.2122+89_2122+93del	XP_011535405.1:n.2122+89_2122+93del
XM_011537104.1:c.2161+89_2161+93del	XP_011535406.1:n.2161+89_2161+93del
NM_006939.3:c.2161+89_2161+93del	NP_008870.2:n.2161+89_2161+93del
NM_006939.4:c.2161+89_2161+93del MANE Select	NP_008870.2:n.2161+89_2161+93del