Canonical Allele Identifier: CA2758614431
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945285_138945286insAAAAAAAAAA , CM000665.2:g.138945285_138945286insAAAAAAAAAA GRCh38
NC_000003.11:g.138664127_138664128insAAAAAAAAAA , CM000665.1:g.138664127_138664128insAAAAAAAAAA GRCh37
NC_000003.10:g.140146817_140146818insAAAAAAAAAA NCBI36
NG_012454.1:g.6856_6857insTTTTTTTTTT
NG_029796.1:g.3052_3053insAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*307_*308insTTTTTTTTTT MANE Select ENSP00000497217.1:n.*307_*308insTTTTTTTTTT
ENST00000330315.3:c.*307_*308insTTTTTTTTTT ENSP00000333188.3:n.*307_*308insTTTTTTTTTT
NM_023067.3:c.*307_*308insTTTTTTTTTT NP_075555.1:n.*307_*308insTTTTTTTTTT
NM_023067.4:c.*307_*308insTTTTTTTTTT MANE Select NP_075555.1:n.*307_*308insTTTTTTTTTT