Canonical Allele Identifier: CA2800787194

Gene: OSGEP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454792_20454793insATCCACGTCCAAGT , CM000676.2:g.20454792_20454793insATCCACGTCCAAGT	GRCh38
NC_000014.8:g.20922951_20922952insATCCACGTCCAAGT , CM000676.1:g.20922951_20922952insATCCACGTCCAAGT	GRCh37
NC_000014.7:g.19992791_19992792insATCCACGTCCAAGT	NCBI36
NG_008718.1:g.4662_4663insATCCACGTCCAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.-110_-109insACTTGGACGTGGAT MANE Select	ENSP00000206542.4:n.-110_-109insACTTGGACGTGGAT
ENST00000206542.8:c.-110_-109insACTTGGACGTGGAT	ENSP00000206542.4:n.-110_-109insACTTGGACGTGGAT
ENST00000553640.3:c.-110_-109insACTTGGACGTGGAT	ENSP00000451580.1:n.-110_-109insACTTGGACGTGGAT
ENST00000554699.1:n.1_2insACTTGGACGTGGAT
ENST00000556252.1:n.261_262insACTTGGACGTGGAT
ENST00000556439.1:n.297_298insACTTGGACGTGGAT
NM_017807.3:c.-110_-109insACTTGGACGTGGAT	NP_060277.1:n.-110_-109insACTTGGACGTGGAT
XM_011536930.1:c.-171_-170insACTTGGACGTGGAT	XP_011535232.1:n.-171_-170insACTTGGACGTGGAT
XM_011536931.1:c.-406_-405insACTTGGACGTGGAT	XP_011535233.1:n.-406_-405insACTTGGACGTGGAT
XM_011536932.1:c.-410_-409insACTTGGACGTGGAT	XP_011535234.1:n.-410_-409insACTTGGACGTGGAT
NM_017807.4:c.-110_-109insACTTGGACGTGGAT MANE Select	NP_060277.1:n.-110_-109insACTTGGACGTGGAT