Canonical Allele Identifier: CA2586973031
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946096del , CM000665.2:g.138946096del GRCh38
NC_000003.11:g.138664938del , CM000665.1:g.138664938del GRCh37
NC_000003.10:g.140147628del NCBI36
NG_012454.1:g.6045del
NG_029796.1:g.3863del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.627del MANE Select ENSP00000497217.1:p.Ser211HisfsTer?
ENST00000330315.3:c.627del ENSP00000333188.3:p.Ser211HisfsTer?
NM_023067.3:c.627del NP_075555.1:p.Ser211HisfsTer?
NM_023067.4:c.627del MANE Select NP_075555.1:p.Ser211HisfsTer?