Canonical Allele Identifier: CA1405401995
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945619_138945620delinsGC , CM000665.2:g.138945619_138945620delinsGC GRCh38
NC_000003.11:g.138664461_138664462delinsGC , CM000665.1:g.138664461_138664462delinsGC GRCh37
NC_000003.10:g.140147151_140147152delinsGC NCBI36
NG_012454.1:g.6521_6522delinsGC
NG_029796.1:g.3386_3387delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1103_1104delinsGC MANE Select ENSP00000497217.1:p.Gly368=
ENST00000330315.3:c.1103_1104delinsGC ENSP00000333188.3:p.Gly368=
NM_023067.3:c.1103_1104delinsGC NP_075555.1:p.Gly368=
NM_023067.4:c.1103_1104delinsGC MANE Select NP_075555.1:p.Gly368=
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