Canonical Allele Identifier: CA2575539815

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180663_50180664del , CM000676.2:g.50180663_50180664del	GRCh38
NC_000014.8:g.50647381_50647382del , CM000676.1:g.50647381_50647382del	GRCh37
NC_000014.7:g.49717131_49717132del	NCBI36
NG_051073.1:g.56031_56032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.878_879del MANE Select	ENSP00000216373.5:p.Tyr293Ter
ENST00000216373.9:c.878_879del	ENSP00000216373.5:p.Tyr293Ter
ENST00000543680.5:c.878_879del	ENSP00000445328.1:p.Tyr293Ter
NM_006939.2:c.878_879del	NP_008870.2:p.Tyr293Ter
XM_005268021.1:c.698_699del	XP_005268078.1:p.Tyr233Ter
XM_011537103.1:c.839_840del	XP_011535405.1:p.Tyr280Ter
XM_011537104.1:c.878_879del	XP_011535406.1:p.Tyr293Ter
XR_943842.1:n.954-3124_954-3123del
XR_943843.1:n.954-3124_954-3123del
NM_006939.3:c.878_879del	NP_008870.2:p.Tyr293Ter
NM_006939.4:c.878_879del MANE Select	NP_008870.2:p.Tyr293Ter