Canonical Allele Identifier: CA2624772503

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180707-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180707_50180708insG , CM000676.2:g.50180707_50180708insG	GRCh38
NC_000014.8:g.50647425_50647426insG , CM000676.1:g.50647425_50647426insG	GRCh37
NC_000014.7:g.49717175_49717176insG	NCBI36
NG_051073.1:g.55986_55987insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-26_859-25insC MANE Select	ENSP00000216373.5:n.859-26_859-25insC
ENST00000216373.9:c.859-26_859-25insC	ENSP00000216373.5:n.859-26_859-25insC
ENST00000543680.5:c.859-26_859-25insC	ENSP00000445328.1:n.859-26_859-25insC
NM_006939.2:c.859-26_859-25insC	NP_008870.2:n.859-26_859-25insC
XM_005268021.1:c.679-26_679-25insC	XP_005268078.1:n.679-26_679-25insC
XM_011537103.1:c.820-26_820-25insC	XP_011535405.1:n.820-26_820-25insC
XM_011537104.1:c.859-26_859-25insC	XP_011535406.1:n.859-26_859-25insC
XR_943842.1:n.954-3080_954-3079insG
XR_943843.1:n.954-3080_954-3079insG
NM_006939.3:c.859-26_859-25insC	NP_008870.2:n.859-26_859-25insC
NM_006939.4:c.859-26_859-25insC MANE Select	NP_008870.2:n.859-26_859-25insC