Canonical Allele Identifier: CA2843177593
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945717_138945718insCCACCA , CM000665.2:g.138945717_138945718insCCACCA GRCh38
NC_000003.11:g.138664559_138664560insCCACCA , CM000665.1:g.138664559_138664560insCCACCA GRCh37
NC_000003.10:g.140147249_140147250insCCACCA NCBI36
NG_012454.1:g.6423_6424insTGGTGG
NG_029796.1:g.3484_3485insCCACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1005_1006insTGGTGG MANE Select ENSP00000497217.1:p.Pro335_Ala336insTrpTrp
ENST00000330315.3:c.1005_1006insTGGTGG ENSP00000333188.3:p.Pro335_Ala336insTrpTrp
NM_023067.3:c.1005_1006insTGGTGG NP_075555.1:p.Pro335_Ala336insTrpTrp
NM_023067.4:c.1005_1006insTGGTGG MANE Select NP_075555.1:p.Pro335_Ala336insTrpTrp
Search 100 bp 5'
Search 100 bp 3'