Canonical Allele Identifier: CA2586973012

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945836dup , CM000665.2:g.138945836dup	GRCh38
NC_000003.11:g.138664678dup , CM000665.1:g.138664678dup	GRCh37
NC_000003.10:g.140147368dup	NCBI36
NG_012454.1:g.6305dup
NG_029796.1:g.3603dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.887dup MANE Select	ENSP00000497217.1:p.His297ThrfsTer?
ENST00000330315.3:c.887dup	ENSP00000333188.3:p.His297ThrfsTer?
NM_023067.3:c.887dup	NP_075555.1:p.His297ThrfsTer?
NM_023067.4:c.887dup MANE Select	NP_075555.1:p.His297ThrfsTer?