Canonical Allele Identifier: CA1405402151
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945767_138945775delinsGGCGGCGGC , CM000665.2:g.138945767_138945775delinsGGCGGCGGC GRCh38
NC_000003.11:g.138664609_138664617delinsGGCGGCGGC , CM000665.1:g.138664609_138664617delinsGGCGGCGGC GRCh37
NC_000003.10:g.140147299_140147307delinsGGCGGCGGC NCBI36
NG_012454.1:g.6366_6374delinsGCCGCCGCC
NG_029796.1:g.3534_3542delinsGGCGGCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.948_956delinsGCCGCCGCC MANE Select ENSP00000497217.1:p.Ala316=
ENST00000330315.3:c.948_956delinsGCCGCCGCC ENSP00000333188.3:p.Ala316=
NM_023067.3:c.948_956delinsGCCGCCGCC NP_075555.1:p.Ala316=
NM_023067.4:c.948_956delinsGCCGCCGCC MANE Select NP_075555.1:p.Ala316=
Search 100 bp 5'
Search 100 bp 3'