Canonical Allele Identifier: CA2624005920
Gene: OSGEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454799_20454819del , CM000676.2:g.20454799_20454819del GRCh38
NC_000014.8:g.20922958_20922978del , CM000676.1:g.20922958_20922978del GRCh37
NC_000014.7:g.19992798_19992818del NCBI36
NG_008718.1:g.4669_4689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-136_-116del ENSP00000206542.4:n.-136_-116del
ENST00000556252.1:n.235_255del
ENST00000556439.1:n.271_291del
NM_017807.3:c.-136_-116del NP_060277.1:n.-136_-116del
XM_011536930.1:c.-197_-177del XP_011535232.1:n.-197_-177del
XM_011536931.1:c.-432_-412del XP_011535233.1:n.-432_-412del