Canonical Allele Identifier: CA2759648174
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713572_181713573insGGTT , CM000665.2:g.181713572_181713573insGGTT GRCh38
NC_000003.11:g.181431360_181431361insGGTT , CM000665.1:g.181431360_181431361insGGTT GRCh37
NC_000003.10:g.182914054_182914055insGGTT NCBI36
NG_009080.1:g.6639_6640insGGTT , LRG_719:g.6639_6640insGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*258_*259insGGTT (SOX2) MANE Select ENSP00000323588.1:n.*258_*259insGGTT
ENST00000325404.2:c.*258_*259insGGTT (SOX2) ENSP00000323588.1:n.*258_*259insGGTT
NM_003106.3:c.*258_*259insGGTT (SOX2) NP_003097.1:n.*258_*259insGGTT
NR_004053.3:n.768-1613_768-1612insGGTT (SOX2-OT)
NR_075089.1:n.767+13689_767+13690insGGTT (SOX2-OT)
NR_075090.1:n.482-25997_482-25996insGGTT (SOX2-OT)
NR_075091.1:n.783-1613_783-1612insGGTT (SOX2-OT)
NR_075092.1:n.782+13689_782+13690insGGTT (SOX2-OT)
NR_075093.1:n.473-25997_473-25996insGGTT (SOX2-OT)
NM_003106.4:c.*258_*259insGGTT (SOX2) MANE Select NP_003097.1:n.*258_*259insGGTT