Canonical Allele Identifier: CA960844078
Gene: OSGEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20452587_20452588insAATGATACGGCGAC , CM000676.2:g.20452587_20452588insAATGATACGGCGAC GRCh38
NC_000014.8:g.20920746_20920747insAATGATACGGCGAC , CM000676.1:g.20920746_20920747insAATGATACGGCGAC GRCh37
NC_000014.7:g.19990586_19990587insAATGATACGGCGAC NCBI36
NG_008718.1:g.2457_2458insAATGATACGGCGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.9:c.116-140_116-139insGTCGCCGTATCATT MANE Select ENSP00000206542.4:n.116-140_116-139insGTCGCCGTATCATT
ENST00000206542.8:c.116-140_116-139insGTCGCCGTATCATT ENSP00000206542.4:n.116-140_116-139insGTCGCCGTATCATT
ENST00000553640.3:c.116-140_116-139insGTCGCCGTATCATT ENSP00000451580.1:n.116-140_116-139insGTCGCCGTATCATT
ENST00000554699.1:n.226-140_226-139insGTCGCCGTATCATT
ENST00000556252.1:n.486-140_486-139insGTCGCCGTATCATT
ENST00000556439.1:n.522-140_522-139insGTCGCCGTATCATT
NM_017807.3:c.116-140_116-139insGTCGCCGTATCATT NP_060277.1:n.116-140_116-139insGTCGCCGTATCATT
XM_011536930.1:c.59-140_59-139insGTCGCCGTATCATT XP_011535232.1:n.59-140_59-139insGTCGCCGTATCATT
XM_011536931.1:c.-181-140_-181-139insGTCGCCGTATCATT XP_011535233.1:n.-181-140_-181-139insGTCGCCGTATCATT
XM_011536932.1:c.-181-140_-181-139insGTCGCCGTATCATT XP_011535234.1:n.-181-140_-181-139insGTCGCCGTATCATT
NM_017807.4:c.116-140_116-139insGTCGCCGTATCATT MANE Select NP_060277.1:n.116-140_116-139insGTCGCCGTATCATT