Canonical Allele Identifier: CA2122037877

Gene: OSGEP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454793G= , CM000676.2:g.20454793G=	GRCh38
NC_000014.8:g.20922952G= , CM000676.1:g.20922952G=	GRCh37
NC_000014.7:g.19992792G=	NCBI36
NG_008718.1:g.4663G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.-110C= MANE Select	ENSP00000206542.4:n.-110C=
ENST00000206542.8:c.-110C=	ENSP00000206542.4:n.-110C=
ENST00000553640.3:c.-110C=	ENSP00000451580.1:n.-110C=
ENST00000554699.1:n.1C=
ENST00000556252.1:n.261C=
ENST00000556439.1:n.297C=
NM_017807.3:c.-110C=	NP_060277.1:n.-110C=
XM_011536930.1:c.-171C=	XP_011535232.1:n.-171C=
XM_011536931.1:c.-406C=	XP_011535233.1:n.-406C=
XM_011536932.1:c.-410C=	XP_011535234.1:n.-410C=
NM_017807.4:c.-110C= MANE Select	NP_060277.1:n.-110C=