Canonical Allele Identifier: CA2586973023

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138946014-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946018del , CM000665.2:g.138946018del	GRCh38
NC_000003.11:g.138664860del , CM000665.1:g.138664860del	GRCh37
NC_000003.10:g.140147550del	NCBI36
NG_012454.1:g.6126del
NG_029796.1:g.3785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.708del MANE Select	ENSP00000497217.1:p.Gly237ValfsTer?
ENST00000330315.3:c.708del	ENSP00000333188.3:p.Gly237ValfsTer?
NM_023067.3:c.708del	NP_075555.1:p.Gly237ValfsTer?
NM_023067.4:c.708del MANE Select	NP_075555.1:p.Gly237ValfsTer?