Canonical Allele Identifier: CA2624772109

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180545-A-AAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180547_50180548insCAA , CM000676.2:g.50180547_50180548insCAA	GRCh38
NC_000014.8:g.50647265_50647266insCAA , CM000676.1:g.50647265_50647266insCAA	GRCh37
NC_000014.7:g.49717015_49717016insCAA	NCBI36
NG_051073.1:g.56148_56149insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.969+26_969+27insGTT MANE Select	ENSP00000216373.5:n.969+26_969+27insGTT
ENST00000216373.9:c.969+26_969+27insGTT	ENSP00000216373.5:n.969+26_969+27insGTT
ENST00000543680.5:c.969+26_969+27insGTT	ENSP00000445328.1:n.969+26_969+27insGTT
ENST00000555794.2:c.83+26_83+27insGTT
NM_006939.2:c.969+26_969+27insGTT	NP_008870.2:n.969+26_969+27insGTT
XM_005268021.1:c.789+26_789+27insGTT	XP_005268078.1:n.789+26_789+27insGTT
XM_011537103.1:c.930+26_930+27insGTT	XP_011535405.1:n.930+26_930+27insGTT
XM_011537104.1:c.969+26_969+27insGTT	XP_011535406.1:n.969+26_969+27insGTT
XR_943842.1:n.954-3240_954-3239insCAA
XR_943843.1:n.954-3240_954-3239insCAA
NM_006939.3:c.969+26_969+27insGTT	NP_008870.2:n.969+26_969+27insGTT
NM_006939.4:c.969+26_969+27insGTT MANE Select	NP_008870.2:n.969+26_969+27insGTT