Canonical Allele Identifier: CA2586973045
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946435del , CM000665.2:g.138946435del GRCh38
NC_000003.11:g.138665277del , CM000665.1:g.138665277del GRCh37
NC_000003.10:g.140147967del NCBI36
NG_012454.1:g.5708del
NG_029796.1:g.4202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.290del MANE Select ENSP00000497217.1:p.Gly97AlafsTer?
ENST00000330315.3:c.290del ENSP00000333188.3:p.Gly97AlafsTer?
NM_023067.3:c.290del NP_075555.1:p.Gly97AlafsTer?
NM_023067.4:c.290del MANE Select NP_075555.1:p.Gly97AlafsTer?