Canonical Allele Identifier: CA2580068845
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2203451
ClinVar RCV Id: RCV002651753

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945967_138945974del , CM000665.2:g.138945967_138945974del GRCh38
NC_000003.11:g.138664809_138664816del , CM000665.1:g.138664809_138664816del GRCh37
NC_000003.10:g.140147499_140147506del NCBI36
NG_012454.1:g.6170_6177del
NG_029796.1:g.3734_3741del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.752_759del MANE Select ENSP00000497217.1:p.Pro251LeufsTer?
ENST00000330315.3:c.752_759del ENSP00000333188.3:p.Pro251LeufsTer?
NM_023067.3:c.752_759del NP_075555.1:p.Pro251LeufsTer?
NM_023067.4:c.752_759del MANE Select NP_075555.1:p.Pro251LeufsTer?