Canonical Allele Identifier: CA2624771480

Gene: SOS2

Linked Data

• gnomAD v4: 14-50153132-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153137del , CM000676.2:g.50153137del	GRCh38
NC_000014.8:g.50619855del , CM000676.1:g.50619855del	GRCh37
NC_000014.7:g.49689605del	NCBI36
NG_051073.1:g.83561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2098del MANE Select	ENSP00000216373.5:p.Tyr700MetfsTer13
ENST00000216373.9:c.2098del	ENSP00000216373.5:p.Tyr700MetfsTer13
ENST00000543680.5:c.1999del	ENSP00000445328.1:p.Tyr667MetfsTer13
NM_006939.2:c.2098del	NP_008870.2:p.Tyr700MetfsTer13
XM_005268021.1:c.1918del	XP_005268078.1:p.Tyr640MetfsTer13
XM_011537103.1:c.2059del	XP_011535405.1:p.Tyr687MetfsTer13
XM_011537104.1:c.2098del	XP_011535406.1:p.Tyr700MetfsTer13
NM_006939.3:c.2098del	NP_008870.2:p.Tyr700MetfsTer13
NM_006939.4:c.2098del MANE Select	NP_008870.2:p.Tyr700MetfsTer13