Canonical Allele Identifier: CA2667924632

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945260-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945260_138945261insG , CM000665.2:g.138945260_138945261insG	GRCh38
NC_000003.11:g.138664102_138664103insG , CM000665.1:g.138664102_138664103insG	GRCh37
NC_000003.10:g.140146792_140146793insG	NCBI36
NG_012454.1:g.6880_6881insC
NG_029796.1:g.3027_3028insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*331_*332insC MANE Select	ENSP00000497217.1:n.*331_*332insC
ENST00000330315.3:c.*331_*332insC	ENSP00000333188.3:n.*331_*332insC
NM_023067.3:c.*331_*332insC	NP_075555.1:n.*331_*332insC
NM_023067.4:c.*331_*332insC MANE Select	NP_075555.1:n.*331_*332insC