Canonical Allele Identifier: CA2122037948
Gene: OSGEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454821C= , CM000676.2:g.20454821C= GRCh38
NC_000014.8:g.20922980C= , CM000676.1:g.20922980C= GRCh37
NC_000014.7:g.19992820C= NCBI36
NG_008718.1:g.4691C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-138G= ENSP00000206542.4:n.-138G=
ENST00000556252.1:n.233G=
ENST00000556439.1:n.269G=
NM_017807.3:c.-138G= NP_060277.1:n.-138G=
XM_011536930.1:c.-199G= XP_011535232.1:n.-199G=
XM_011536931.1:c.-434G= XP_011535233.1:n.-434G=