Canonical Allele Identifier: CA960845153
Gene: OSGEP HGNC NCBI

Linked Data

dbSNP Id: rs1354246013

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454911_20454912insG , CM000676.2:g.20454911_20454912insG GRCh38
NC_000014.8:g.20923070_20923071insG , CM000676.1:g.20923070_20923071insG GRCh37
NC_000014.7:g.19992910_19992911insG NCBI36
NG_008718.1:g.4781_4782insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-229_-228insC ENSP00000206542.4:n.-229_-228insC
ENST00000556252.1:n.142_143insC
ENST00000556439.1:n.178_179insC
NM_017807.3:c.-229_-228insC NP_060277.1:n.-229_-228insC
XM_011536930.1:c.-290_-289insC XP_011535232.1:n.-290_-289insC