Canonical Allele Identifier: CA2841614452

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199833_50199834insTAAATTTAA , CM000676.2:g.50199833_50199834insTAAATTTAA	GRCh38
NC_000014.8:g.50666551_50666552insTAAATTTAA , CM000676.1:g.50666551_50666552insTAAATTTAA	GRCh37
NC_000014.7:g.49736301_49736302insTAAATTTAA	NCBI36
NG_051073.1:g.36860_36861insTTAAATTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.367_368insTTAAATTTA MANE Select	ENSP00000216373.5:p.Asp123delinsValLysPheAsn
ENST00000216373.9:c.367_368insTTAAATTTA	ENSP00000216373.5:p.Asp123delinsValLysPheAsn
ENST00000543680.5:c.367_368insTTAAATTTA	ENSP00000445328.1:p.Asp123delinsValLysPheAsn
ENST00000555666.1:n.546_547insTTAAATTTA
ENST00000556469.5:n.338_339insTTAAATTTA
NM_006939.2:c.367_368insTTAAATTTA	NP_008870.2:p.Asp123delinsValLysPheAsn
XM_005268021.1:c.187_188insTTAAATTTA	XP_005268078.1:p.Asp63delinsValLysPheAsn
XM_011537103.1:c.328_329insTTAAATTTA	XP_011535405.1:p.Asp110delinsValLysPheAsn
XM_011537104.1:c.367_368insTTAAATTTA	XP_011535406.1:p.Asp123delinsValLysPheAsn
XR_943842.1:n.1039+15961_1039+15962insTAAATTTAA
XR_943843.1:n.1039+15961_1039+15962insTAAATTTAA
NM_006939.3:c.367_368insTTAAATTTA	NP_008870.2:p.Asp123delinsValLysPheAsn
NM_006939.4:c.367_368insTTAAATTTA MANE Select	NP_008870.2:p.Asp123delinsValLysPheAsn