Canonical Allele Identifier: CA2557211660

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130473_50130474insCACGTCTTACAGGGTAGCGCGCCCGTGGATCCGGTGAGCTGTGAGGATAGGCGAACGGGTAGGATGGTGGGCGGTGCGCGTGATGCGCGCAGTAATG , CM000676.2:g.50130473_50130474insCACGTCTTACAGGGTAGCGCGCCCGTGGATCCGGTGAGCTGTGAGGATAGGCGAACGGGTAGGATGGTGGGCGGTGCGCGTGATGCGCGCAGTAATG	GRCh38
NC_000014.8:g.50597191_50597192insCACGTCTTACAGGGTAGCGCGCCCGTGGATCCGGTGAGCTGTGAGGATAGGCGAACGGGTAGGATGGTGGGCGGTGCGCGTGATGCGCGCAGTAATG , CM000676.1:g.50597191_50597192insCACGTCTTACAGGGTAGCGCGCCCGTGGATCCGGTGAGCTGTGAGGATAGGCGAACGGGTAGGATGGTGGGCGGTGCGCGTGATGCGCGCAGTAATG	GRCh37
NC_000014.7:g.49666941_49666942insCACGTCTTACAGGGTAGCGCGCCCGTGGATCCGGTGAGCTGTGAGGATAGGCGAACGGGTAGGATGGTGGGCGGTGCGCGTGATGCGCGCAGTAATG	NCBI36
NG_051073.1:g.106220_106221insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG MANE Select	ENSP00000216373.5:n.3337+27_3337+28insCATTACTGCGCGCATCACGCGCA...
ENST00000216373.9:c.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	ENSP00000216373.5:n.3337+27_3337+28insCATTACTGCGCGCATCACGCGCA...
ENST00000543680.5:c.3238+27_3238+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	ENSP00000445328.1:n.3238+27_3238+28insCATTACTGCGCGCATCACGCGCA...
NM_006939.2:c.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	NP_008870.2:n.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCC...
XM_005268021.1:c.3157+27_3157+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	XP_005268078.1:n.3157+27_3157+28insCATTACTGCGCGCATCACGCGCACCG...
XM_011537103.1:c.3298+27_3298+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	XP_011535405.1:n.3298+27_3298+28insCATTACTGCGCGCATCACGCGCACCG...
NM_006939.3:c.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG	NP_008870.2:n.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCC...
NM_006939.4:c.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCCACCATCCTACCCGTTCGCCTATCCTCACAGCTCACCGGATCCACGGGCGCGCTACCCTGTAAGACGTG MANE Select	NP_008870.2:n.3337+27_3337+28insCATTACTGCGCGCATCACGCGCACCGCCC...