Canonical Allele Identifier: CA2667924619

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945257-GGCCCTTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945258_138945265del , CM000665.2:g.138945258_138945265del	GRCh38
NC_000003.11:g.138664100_138664107del , CM000665.1:g.138664100_138664107del	GRCh37
NC_000003.10:g.140146790_140146797del	NCBI36
NG_012454.1:g.6876_6883del
NG_029796.1:g.3025_3032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*327_*334del MANE Select	ENSP00000497217.1:n.*327_*334del
ENST00000330315.3:c.*327_*334del	ENSP00000333188.3:n.*327_*334del
NM_023067.3:c.*327_*334del	NP_075555.1:n.*327_*334del
NM_023067.4:c.*327_*334del MANE Select	NP_075555.1:n.*327_*334del