Canonical Allele Identifier: CA10654856
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369938
ClinVar RCV Id: RCV000408792
dbSNP Id: rs1057516185

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945714del , CM000665.2:g.138945714del GRCh38
NC_000003.11:g.138664556del , CM000665.1:g.138664556del GRCh37
NC_000003.10:g.140147246del NCBI36
NG_012454.1:g.6429del
NG_029796.1:g.3481del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1011del MANE Select ENSP00000497217.1:p.Thr338ProfsTer18
ENST00000330315.3:c.1011del ENSP00000333188.3:p.Thr338ProfsTer18
NM_023067.3:c.1011del NP_075555.1:p.Thr338ProfsTer18
NM_023067.4:c.1011del MANE Select NP_075555.1:p.Thr338ProfsTer18