Canonical Allele Identifier: CA2577918190

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945847del , CM000665.2:g.138945847del	GRCh38
NC_000003.11:g.138664689del , CM000665.1:g.138664689del	GRCh37
NC_000003.10:g.140147379del	NCBI36
NG_012454.1:g.6294del
NG_029796.1:g.3614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.876del MANE Select	ENSP00000497217.1:p.His293IlefsTer?
ENST00000330315.3:c.876del	ENSP00000333188.3:p.His293IlefsTer?
NM_023067.3:c.876del	NP_075555.1:p.His293IlefsTer?
NM_023067.4:c.876del MANE Select	NP_075555.1:p.His293IlefsTer?