Canonical Allele Identifier: CA2586973044
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946431_138946435del , CM000665.2:g.138946431_138946435del GRCh38
NC_000003.11:g.138665273_138665277del , CM000665.1:g.138665273_138665277del GRCh37
NC_000003.10:g.140147963_140147967del NCBI36
NG_012454.1:g.5708_5712del
NG_029796.1:g.4198_4202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.290_294del MANE Select ENSP00000497217.1:p.Gly97AlafsTer3
ENST00000330315.3:c.290_294del ENSP00000333188.3:p.Gly97AlafsTer3
NM_023067.3:c.290_294del NP_075555.1:p.Gly97AlafsTer3
NM_023067.4:c.290_294del MANE Select NP_075555.1:p.Gly97AlafsTer3
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