Canonical Allele Identifier: CA2586973004
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945744_138945757del , CM000665.2:g.138945744_138945757del GRCh38
NC_000003.11:g.138664586_138664599del , CM000665.1:g.138664586_138664599del GRCh37
NC_000003.10:g.140147276_140147289del NCBI36
NG_012454.1:g.6389_6402del
NG_029796.1:g.3511_3524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.971_984del MANE Select ENSP00000497217.1:p.Pro324HisfsTer?
ENST00000330315.3:c.971_984del ENSP00000333188.3:p.Pro324HisfsTer?
NM_023067.3:c.971_984del NP_075555.1:p.Pro324HisfsTer?
NM_023067.4:c.971_984del MANE Select NP_075555.1:p.Pro324HisfsTer?