Canonical Allele Identifier: CA10654857
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369937
ClinVar RCV Id: RCV000408893
dbSNP Id: rs1057516184

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945741del , CM000665.2:g.138945741del GRCh38
NC_000003.11:g.138664583del , CM000665.1:g.138664583del GRCh37
NC_000003.10:g.140147273del NCBI36
NG_012454.1:g.6400del
NG_029796.1:g.3508del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.982del MANE Select ENSP00000497217.1:p.Ala328ProfsTer28
ENST00000330315.3:c.982del ENSP00000333188.3:p.Ala328ProfsTer28
NM_023067.3:c.982del NP_075555.1:p.Ala328ProfsTer28
NM_023067.4:c.982del MANE Select NP_075555.1:p.Ala328ProfsTer28