Canonical Allele Identifier: CA2843640023

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946584_138946585del , CM000665.2:g.138946584_138946585del	GRCh38
NC_000003.11:g.138665426_138665427del , CM000665.1:g.138665426_138665427del	GRCh37
NC_000003.10:g.140148116_140148117del	NCBI36
NG_012454.1:g.5556_5557del
NG_029796.1:g.4351_4352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.138_139del MANE Select	ENSP00000497217.1:p.Lys48AlafsTer?
ENST00000330315.3:c.138_139del	ENSP00000333188.3:p.Lys48AlafsTer?
NM_023067.3:c.138_139del	NP_075555.1:p.Lys48AlafsTer?
NM_023067.4:c.138_139del MANE Select	NP_075555.1:p.Lys48AlafsTer?