Canonical Allele Identifier: CA1405402300
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946027_138946049delinsTGCAGCCGCAGCTGCTGCAGCCG , CM000665.2:g.138946027_138946049delinsTGCAGCCGCAGCTGCTGCAGCCG GRCh38
NC_000003.11:g.138664869_138664891delinsTGCAGCCGCAGCTGCTGCAGCCG , CM000665.1:g.138664869_138664891delinsTGCAGCCGCAGCTGCTGCAGCCG GRCh37
NC_000003.10:g.140147559_140147581delinsTGCAGCCGCAGCTGCTGCAGCCG NCBI36
NG_012454.1:g.6092_6114delinsCGGCTGCAGCAGCTGCGGCTGCA
NG_029796.1:g.3794_3816delinsTGCAGCCGCAGCTGCTGCAGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.674_696delinsCGGCTGCAGCAGCTGCGGCTGCA MANE Select ENSP00000497217.1:p.Ala225=
ENST00000330315.3:c.674_696delinsCGGCTGCAGCAGCTGCGGCTGCA ENSP00000333188.3:p.Ala225=
NM_023067.3:c.674_696delinsCGGCTGCAGCAGCTGCGGCTGCA NP_075555.1:p.Ala225=
NM_023067.4:c.674_696delinsCGGCTGCAGCAGCTGCGGCTGCA MANE Select NP_075555.1:p.Ala225=
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