Canonical Allele Identifier: CA2667924630

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945259-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945260_138945262del , CM000665.2:g.138945260_138945262del	GRCh38
NC_000003.11:g.138664102_138664104del , CM000665.1:g.138664102_138664104del	GRCh37
NC_000003.10:g.140146792_140146794del	NCBI36
NG_012454.1:g.6879_6881del
NG_029796.1:g.3027_3029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*330_*332del MANE Select	ENSP00000497217.1:n.*330_*332del
ENST00000330315.3:c.*330_*332del	ENSP00000333188.3:n.*330_*332del
NM_023067.3:c.*330_*332del	NP_075555.1:n.*330_*332del
NM_023067.4:c.*330_*332del MANE Select	NP_075555.1:n.*330_*332del