Canonical Allele Identifier: CA2542698300

Gene: OSGEP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20452578_20452580del , CM000676.2:g.20452578_20452580del	GRCh38
NC_000014.8:g.20920737_20920739del , CM000676.1:g.20920737_20920739del	GRCh37
NC_000014.7:g.19990577_19990579del	NCBI36
NG_008718.1:g.2448_2450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.116-132_116-130del MANE Select	ENSP00000206542.4:n.116-132_116-130del
ENST00000206542.8:c.116-132_116-130del	ENSP00000206542.4:n.116-132_116-130del
ENST00000553640.3:c.116-132_116-130del	ENSP00000451580.1:n.116-132_116-130del
ENST00000554699.1:n.226-132_226-130del
ENST00000556252.1:n.486-132_486-130del
ENST00000556439.1:n.522-132_522-130del
NM_017807.3:c.116-132_116-130del	NP_060277.1:n.116-132_116-130del
XM_011536930.1:c.59-132_59-130del	XP_011535232.1:n.59-132_59-130del
XM_011536931.1:c.-181-132_-181-130del	XP_011535233.1:n.-181-132_-181-130del
XM_011536932.1:c.-181-132_-181-130del	XP_011535234.1:n.-181-132_-181-130del
NM_017807.4:c.116-132_116-130del MANE Select	NP_060277.1:n.116-132_116-130del