Canonical Allele Identifier: CA7081107

Gene: OSGEP

Linked Data

• ClinVar Variation Id: 444893
• ClinVar RCV Id: RCV000512759 ; RCV001849393 ; RCV002524976
• dbSNP Id: rs773173317
• ExAC: 14:20916116 C / T
• gnomAD v2: 14-20916116-C-T
• gnomAD v3: 14-20447957-C-T
• gnomAD v4: 14-20447957-C-T
• MyVariant Identifiers: chr14:g.20916116C>T (hg19) ; chr14:g.20447957C>T (hg38)
• PubMed: PMID:11519896 ; PMID:15966048 ; PMID:18019379 ; PMID:21791310 ; PMID:28805828

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20447957C>T , CM000676.2:g.20447957C>T	GRCh38
NC_000014.8:g.20916116C>T , CM000676.1:g.20916116C>T	GRCh37
NC_000014.7:g.19985956C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.740G>A MANE Select	ENSP00000206542.4:p.Arg247Gln
ENST00000206542.8:c.740G>A	ENSP00000206542.4:p.Arg247Gln
ENST00000554249.5:n.618G>A
ENST00000555223.5:c.660G>A
ENST00000555656.5:n.2161G>A
ENST00000555785.2:n.398G>A
ENST00000556124.3:n.888G>A
NM_017807.3:c.740G>A	NP_060277.1:p.Arg247Gln
XM_011536930.1:c.683G>A	XP_011535232.1:p.Arg228Gln
XM_011536931.1:c.497G>A	XP_011535233.1:p.Arg166Gln
XM_011536932.1:c.497G>A	XP_011535234.1:p.Arg166Gln
NM_017807.4:c.740G>A MANE Select	NP_060277.1:p.Arg247Gln