Canonical Allele Identifier: CA2667925934
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945973del , CM000665.2:g.138945973del GRCh38
NC_000003.11:g.138664815del , CM000665.1:g.138664815del GRCh37
NC_000003.10:g.140147505del NCBI36
NG_012454.1:g.6170del
NG_029796.1:g.3740del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.752del MANE Select ENSP00000497217.1:p.Pro251ArgfsTer20
ENST00000330315.3:c.752del ENSP00000333188.3:p.Pro251ArgfsTer20
NM_023067.3:c.752del NP_075555.1:p.Pro251ArgfsTer20
NM_023067.4:c.752del MANE Select NP_075555.1:p.Pro251ArgfsTer20