Canonical Allele Identifier: CA2624005909

Gene: OSGEP

Linked Data

• gnomAD v4: 14-20454794-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454794C>T , CM000676.2:g.20454794C>T	GRCh38
NC_000014.8:g.20922953C>T , CM000676.1:g.20922953C>T	GRCh37
NC_000014.7:g.19992793C>T	NCBI36
NG_008718.1:g.4664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.9:c.-111G>A MANE Select	ENSP00000206542.4:n.-111G>A
ENST00000206542.8:c.-111G>A	ENSP00000206542.4:n.-111G>A
ENST00000553640.3:c.-111G>A	ENSP00000451580.1:n.-111G>A
ENST00000556252.1:n.260G>A
ENST00000556439.1:n.296G>A
NM_017807.3:c.-111G>A	NP_060277.1:n.-111G>A
XM_011536930.1:c.-172G>A	XP_011535232.1:n.-172G>A
XM_011536931.1:c.-407G>A	XP_011535233.1:n.-407G>A
XM_011536932.1:c.-411G>A	XP_011535234.1:n.-411G>A
NM_017807.4:c.-111G>A MANE Select	NP_060277.1:n.-111G>A