Canonical Allele Identifier: CA2136084836

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180842_50180843delinsCA , CM000676.2:g.50180842_50180843delinsCA	GRCh38
NC_000014.8:g.50647560_50647561delinsCA , CM000676.1:g.50647560_50647561delinsCA	GRCh37
NC_000014.7:g.49717310_49717311delinsCA	NCBI36
NG_051073.1:g.55851_55852delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-161_859-160delinsTG MANE Select	ENSP00000216373.5:n.859-161_859-160delinsTG
ENST00000216373.9:c.859-161_859-160delinsTG	ENSP00000216373.5:n.859-161_859-160delinsTG
ENST00000543680.5:c.859-161_859-160delinsTG	ENSP00000445328.1:n.859-161_859-160delinsTG
NM_006939.2:c.859-161_859-160delinsTG	NP_008870.2:n.859-161_859-160delinsTG
XM_005268021.1:c.679-161_679-160delinsTG	XP_005268078.1:n.679-161_679-160delinsTG
XM_011537103.1:c.820-161_820-160delinsTG	XP_011535405.1:n.820-161_820-160delinsTG
XM_011537104.1:c.859-161_859-160delinsTG	XP_011535406.1:n.859-161_859-160delinsTG
XR_943842.1:n.954-2945_954-2944delinsCA
XR_943843.1:n.954-2945_954-2944delinsCA
NM_006939.3:c.859-161_859-160delinsTG	NP_008870.2:n.859-161_859-160delinsTG
NM_006939.4:c.859-161_859-160delinsTG MANE Select	NP_008870.2:n.859-161_859-160delinsTG