Canonical Allele Identifier: CA1405402135
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945742_138945751delinsTGGGCTGGCA , CM000665.2:g.138945742_138945751delinsTGGGCTGGCA GRCh38
NC_000003.11:g.138664584_138664593delinsTGGGCTGGCA , CM000665.1:g.138664584_138664593delinsTGGGCTGGCA GRCh37
NC_000003.10:g.140147274_140147283delinsTGGGCTGGCA NCBI36
NG_012454.1:g.6390_6399delinsTGCCAGCCCA
NG_029796.1:g.3509_3518delinsTGGGCTGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.972_981delinsTGCCAGCCCA MANE Select ENSP00000497217.1:p.Pro324=
ENST00000330315.3:c.972_981delinsTGCCAGCCCA ENSP00000333188.3:p.Pro324=
NM_023067.3:c.972_981delinsTGCCAGCCCA NP_075555.1:p.Pro324=
NM_023067.4:c.972_981delinsTGCCAGCCCA MANE Select NP_075555.1:p.Pro324=
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