Canonical Allele Identifier: CA1405402469
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946335_138946336delinsGC , CM000665.2:g.138946335_138946336delinsGC GRCh38
NC_000003.11:g.138665177_138665178delinsGC , CM000665.1:g.138665177_138665178delinsGC GRCh37
NC_000003.10:g.140147867_140147868delinsGC NCBI36
NG_012454.1:g.5805_5806delinsGC
NG_029796.1:g.4102_4103delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.387_388delinsGC MANE Select ENSP00000497217.1:p.Thr129=
ENST00000330315.3:c.387_388delinsGC ENSP00000333188.3:p.Thr129=
NM_023067.3:c.387_388delinsGC NP_075555.1:p.Thr129=
NM_023067.4:c.387_388delinsGC MANE Select NP_075555.1:p.Thr129=
Search 100 bp 5'
Search 100 bp 3'