Canonical Allele Identifier: CA1405402112
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945711_138945726delinsTGGGCGCGGGCGCCGG , CM000665.2:g.138945711_138945726delinsTGGGCGCGGGCGCCGG GRCh38
NC_000003.11:g.138664553_138664568delinsTGGGCGCGGGCGCCGG , CM000665.1:g.138664553_138664568delinsTGGGCGCGGGCGCCGG GRCh37
NC_000003.10:g.140147243_140147258delinsTGGGCGCGGGCGCCGG NCBI36
NG_012454.1:g.6415_6430delinsCCGGCGCCCGCGCCCA
NG_029796.1:g.3478_3493delinsTGGGCGCGGGCGCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.997_1012delinsCCGGCGCCCGCGCCCA MANE Select ENSP00000497217.1:p.Pro333=
ENST00000330315.3:c.997_1012delinsCCGGCGCCCGCGCCCA ENSP00000333188.3:p.Pro333=
NM_023067.3:c.997_1012delinsCCGGCGCCCGCGCCCA NP_075555.1:p.Pro333=
NM_023067.4:c.997_1012delinsCCGGCGCCCGCGCCCA MANE Select NP_075555.1:p.Pro333=
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