Canonical Allele Identifier: CA2667926184

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138946036-AGCTGCTGCAGCCGCTGCGGCTGCCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946037_138946061del , CM000665.2:g.138946037_138946061del	GRCh38
NC_000003.11:g.138664879_138664903del , CM000665.1:g.138664879_138664903del	GRCh37
NC_000003.10:g.140147569_140147593del	NCBI36
NG_012454.1:g.6080_6104del
NG_029796.1:g.3804_3828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.662_686del MANE Select	ENSP00000497217.1:p.Ala221ValfsTer?
ENST00000330315.3:c.662_686del	ENSP00000333188.3:p.Ala221ValfsTer?
NM_023067.3:c.662_686del	NP_075555.1:p.Ala221ValfsTer?
NM_023067.4:c.662_686del MANE Select	NP_075555.1:p.Ala221ValfsTer?