Canonical Allele Identifier: CA2136066009

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152964_50152966delinsCAA , CM000676.2:g.50152964_50152966delinsCAA	GRCh38
NC_000014.8:g.50619682_50619684delinsCAA , CM000676.1:g.50619682_50619684delinsCAA	GRCh37
NC_000014.7:g.49689432_49689434delinsCAA	NCBI36
NG_051073.1:g.83728_83730delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+104_2161+106delinsTTG MANE Select	ENSP00000216373.5:n.2161+104_2161+106delinsTTG
ENST00000216373.9:c.2161+104_2161+106delinsTTG	ENSP00000216373.5:n.2161+104_2161+106delinsTTG
ENST00000543680.5:c.2062+104_2062+106delinsTTG	ENSP00000445328.1:n.2062+104_2062+106delinsTTG
NM_006939.2:c.2161+104_2161+106delinsTTG	NP_008870.2:n.2161+104_2161+106delinsTTG
XM_005268021.1:c.1981+104_1981+106delinsTTG	XP_005268078.1:n.1981+104_1981+106delinsTTG
XM_011537103.1:c.2122+104_2122+106delinsTTG	XP_011535405.1:n.2122+104_2122+106delinsTTG
XM_011537104.1:c.2161+104_2161+106delinsTTG	XP_011535406.1:n.2161+104_2161+106delinsTTG
NM_006939.3:c.2161+104_2161+106delinsTTG	NP_008870.2:n.2161+104_2161+106delinsTTG
NM_006939.4:c.2161+104_2161+106delinsTTG MANE Select	NP_008870.2:n.2161+104_2161+106delinsTTG