Canonical Allele Identifier: CA2122035499

Gene: OSGEP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20452561C= , CM000676.2:g.20452561C=	GRCh38
NC_000014.8:g.20920720C= , CM000676.1:g.20920720C=	GRCh37
NC_000014.7:g.19990560C=	NCBI36
NG_008718.1:g.2431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.116-113G= MANE Select	ENSP00000206542.4:n.116-113G=
ENST00000206542.8:c.116-113G=	ENSP00000206542.4:n.116-113G=
ENST00000553640.3:c.116-113G=	ENSP00000451580.1:n.116-113G=
ENST00000554699.1:n.226-113G=
ENST00000556252.1:n.486-113G=
ENST00000556439.1:n.522-113G=
NM_017807.3:c.116-113G=	NP_060277.1:n.116-113G=
XM_011536930.1:c.59-113G=	XP_011535232.1:n.59-113G=
XM_011536931.1:c.-181-113G=	XP_011535233.1:n.-181-113G=
XM_011536932.1:c.-181-113G=	XP_011535234.1:n.-181-113G=
NM_017807.4:c.116-113G= MANE Select	NP_060277.1:n.116-113G=