Canonical Allele Identifier: CA2624772140

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180548-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180549_50180550insGA , CM000676.2:g.50180549_50180550insGA	GRCh38
NC_000014.8:g.50647267_50647268insGA , CM000676.1:g.50647267_50647268insGA	GRCh37
NC_000014.7:g.49717017_49717018insGA	NCBI36
NG_051073.1:g.56145_56146insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.969+23_969+24insCT MANE Select	ENSP00000216373.5:n.969+23_969+24insCT
ENST00000216373.9:c.969+23_969+24insCT	ENSP00000216373.5:n.969+23_969+24insCT
ENST00000543680.5:c.969+23_969+24insCT	ENSP00000445328.1:n.969+23_969+24insCT
ENST00000555794.2:c.83+23_83+24insCT
NM_006939.2:c.969+23_969+24insCT	NP_008870.2:n.969+23_969+24insCT
XM_005268021.1:c.789+23_789+24insCT	XP_005268078.1:n.789+23_789+24insCT
XM_011537103.1:c.930+23_930+24insCT	XP_011535405.1:n.930+23_930+24insCT
XM_011537104.1:c.969+23_969+24insCT	XP_011535406.1:n.969+23_969+24insCT
XR_943842.1:n.954-3238_954-3237insGA
XR_943843.1:n.954-3238_954-3237insGA
NM_006939.3:c.969+23_969+24insCT	NP_008870.2:n.969+23_969+24insCT
NM_006939.4:c.969+23_969+24insCT MANE Select	NP_008870.2:n.969+23_969+24insCT