Canonical Allele Identifier: CA2552319405
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945729del , CM000665.2:g.138945729del GRCh38
NC_000003.11:g.138664571del , CM000665.1:g.138664571del GRCh37
NC_000003.10:g.140147261del NCBI36
NG_012454.1:g.6416del
NG_029796.1:g.3496del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.998del MANE Select ENSP00000497217.1:p.Pro333ArgfsTer23
ENST00000330315.3:c.998del ENSP00000333188.3:p.Pro333ArgfsTer23
NM_023067.3:c.998del NP_075555.1:p.Pro333ArgfsTer23
NM_023067.4:c.998del MANE Select NP_075555.1:p.Pro333ArgfsTer23