Canonical Allele Identifier: CA2624005982

Gene: OSGEP

Linked Data

• gnomAD v4: 14-20452563-CCAAGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20452564_20452569del , CM000676.2:g.20452564_20452569del	GRCh38
NC_000014.8:g.20920723_20920728del , CM000676.1:g.20920723_20920728del	GRCh37
NC_000014.7:g.19990563_19990568del	NCBI36
NG_008718.1:g.2434_2439del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.116-121_116-116del MANE Select	ENSP00000206542.4:n.116-121_116-116del
ENST00000206542.8:c.116-121_116-116del	ENSP00000206542.4:n.116-121_116-116del
ENST00000553640.3:c.116-121_116-116del	ENSP00000451580.1:n.116-121_116-116del
ENST00000554699.1:n.226-121_226-116del
ENST00000556252.1:n.486-121_486-116del
ENST00000556439.1:n.522-121_522-116del
NM_017807.3:c.116-121_116-116del	NP_060277.1:n.116-121_116-116del
XM_011536930.1:c.59-121_59-116del	XP_011535232.1:n.59-121_59-116del
XM_011536931.1:c.-181-121_-181-116del	XP_011535233.1:n.-181-121_-181-116del
XM_011536932.1:c.-181-121_-181-116del	XP_011535234.1:n.-181-121_-181-116del
NM_017807.4:c.116-121_116-116del MANE Select	NP_060277.1:n.116-121_116-116del