Canonical Allele Identifier: CA1405402032

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945329_138945331delinsCAG , CM000665.2:g.138945329_138945331delinsCAG	GRCh38
NC_000003.11:g.138664171_138664173delinsCAG , CM000665.1:g.138664171_138664173delinsCAG	GRCh37
NC_000003.10:g.140146861_140146863delinsCAG	NCBI36
NG_012454.1:g.6810_6812delinsCTG
NG_029796.1:g.3096_3098delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*261_*263delinsCTG MANE Select	ENSP00000497217.1:n.*261_*263delinsCTG
ENST00000330315.3:c.*261_*263delinsCTG	ENSP00000333188.3:n.*261_*263delinsCTG
NM_023067.3:c.*261_*263delinsCTG	NP_075555.1:n.*261_*263delinsCTG
NM_023067.4:c.*261_*263delinsCTG MANE Select	NP_075555.1:n.*261_*263delinsCTG