Canonical Allele Identifier: CA2843640025

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946608dup , CM000665.2:g.138946608dup	GRCh38
NC_000003.11:g.138665450dup , CM000665.1:g.138665450dup	GRCh37
NC_000003.10:g.140148140dup	NCBI36
NG_012454.1:g.5537dup
NG_029796.1:g.4375dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.119dup MANE Select	ENSP00000497217.1:p.Gly41TrpfsTer?
ENST00000330315.3:c.119dup	ENSP00000333188.3:p.Gly41TrpfsTer?
NM_023067.3:c.119dup	NP_075555.1:p.Gly41TrpfsTer?
NM_023067.4:c.119dup MANE Select	NP_075555.1:p.Gly41TrpfsTer?