Canonical Allele Identifier: CA1405402054
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945644_138945650delinsTAAGAGC , CM000665.2:g.138945644_138945650delinsTAAGAGC GRCh38
NC_000003.11:g.138664486_138664492delinsTAAGAGC , CM000665.1:g.138664486_138664492delinsTAAGAGC GRCh37
NC_000003.10:g.140147176_140147182delinsTAAGAGC NCBI36
NG_012454.1:g.6491_6497delinsGCTCTTA
NG_029796.1:g.3411_3417delinsTAAGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1073_1079delinsGCTCTTA MANE Select ENSP00000497217.1:p.Cys358=
ENST00000330315.3:c.1073_1079delinsGCTCTTA ENSP00000333188.3:p.Cys358=
NM_023067.3:c.1073_1079delinsGCTCTTA NP_075555.1:p.Cys358=
NM_023067.4:c.1073_1079delinsGCTCTTA MANE Select NP_075555.1:p.Cys358=
Search 100 bp 5'
Search 100 bp 3'