Canonical Allele Identifier: CA2667924649

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945263-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945263_138945264insG , CM000665.2:g.138945263_138945264insG	GRCh38
NC_000003.11:g.138664105_138664106insG , CM000665.1:g.138664105_138664106insG	GRCh37
NC_000003.10:g.140146795_140146796insG	NCBI36
NG_012454.1:g.6877_6878insC
NG_029796.1:g.3030_3031insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*328_*329insC MANE Select	ENSP00000497217.1:n.*328_*329insC
ENST00000330315.3:c.*328_*329insC	ENSP00000333188.3:n.*328_*329insC
NM_023067.3:c.*328_*329insC	NP_075555.1:n.*328_*329insC
NM_023067.4:c.*328_*329insC MANE Select	NP_075555.1:n.*328_*329insC