Canonical Allele Identifier: CA2575520452

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153041_50153042insTT , CM000676.2:g.50153041_50153042insTT	GRCh38
NC_000014.8:g.50619759_50619760insTT , CM000676.1:g.50619759_50619760insTT	GRCh37
NC_000014.7:g.49689509_49689510insTT	NCBI36
NG_051073.1:g.83652_83653insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2161+28_2161+29insAA MANE Select	ENSP00000216373.5:n.2161+28_2161+29insAA
ENST00000216373.9:c.2161+28_2161+29insAA	ENSP00000216373.5:n.2161+28_2161+29insAA
ENST00000543680.5:c.2062+28_2062+29insAA	ENSP00000445328.1:n.2062+28_2062+29insAA
NM_006939.2:c.2161+28_2161+29insAA	NP_008870.2:n.2161+28_2161+29insAA
XM_005268021.1:c.1981+28_1981+29insAA	XP_005268078.1:n.1981+28_1981+29insAA
XM_011537103.1:c.2122+28_2122+29insAA	XP_011535405.1:n.2122+28_2122+29insAA
XM_011537104.1:c.2161+28_2161+29insAA	XP_011535406.1:n.2161+28_2161+29insAA
NM_006939.3:c.2161+28_2161+29insAA	NP_008870.2:n.2161+28_2161+29insAA
NM_006939.4:c.2161+28_2161+29insAA MANE Select	NP_008870.2:n.2161+28_2161+29insAA