Canonical Allele Identifier: CA2667924650

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945264-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945264_138945265insGG , CM000665.2:g.138945264_138945265insGG	GRCh38
NC_000003.11:g.138664106_138664107insGG , CM000665.1:g.138664106_138664107insGG	GRCh37
NC_000003.10:g.140146796_140146797insGG	NCBI36
NG_012454.1:g.6876_6877insCC
NG_029796.1:g.3031_3032insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*327_*328insCC MANE Select	ENSP00000497217.1:n.*327_*328insCC
ENST00000330315.3:c.*327_*328insCC	ENSP00000333188.3:n.*327_*328insCC
NM_023067.3:c.*327_*328insCC	NP_075555.1:n.*327_*328insCC
NM_023067.4:c.*327_*328insCC MANE Select	NP_075555.1:n.*327_*328insCC