Canonical Allele Identifier: CA2758614425
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945279_138945280insATTAAAAAA , CM000665.2:g.138945279_138945280insATTAAAAAA GRCh38
NC_000003.11:g.138664121_138664122insATTAAAAAA , CM000665.1:g.138664121_138664122insATTAAAAAA GRCh37
NC_000003.10:g.140146811_140146812insATTAAAAAA NCBI36
NG_012454.1:g.6861_6862insTTTTTTAAT
NG_029796.1:g.3046_3047insATTAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*312_*313insTTTTTTAAT MANE Select ENSP00000497217.1:n.*312_*313insTTTTTTAAT
ENST00000330315.3:c.*312_*313insTTTTTTAAT ENSP00000333188.3:n.*312_*313insTTTTTTAAT
NM_023067.3:c.*312_*313insTTTTTTAAT NP_075555.1:n.*312_*313insTTTTTTAAT
NM_023067.4:c.*312_*313insTTTTTTAAT MANE Select NP_075555.1:n.*312_*313insTTTTTTAAT