Canonical Allele Identifier: CA2758614427
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945283_138945284insTAAAAAAAAAA , CM000665.2:g.138945283_138945284insTAAAAAAAAAA GRCh38
NC_000003.11:g.138664125_138664126insTAAAAAAAAAA , CM000665.1:g.138664125_138664126insTAAAAAAAAAA GRCh37
NC_000003.10:g.140146815_140146816insTAAAAAAAAAA NCBI36
NG_012454.1:g.6857_6858insTTTTTTTTTTA
NG_029796.1:g.3050_3051insTAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*308_*309insTTTTTTTTTTA MANE Select ENSP00000497217.1:n.*308_*309insTTTTTTTTTTA
ENST00000330315.3:c.*308_*309insTTTTTTTTTTA ENSP00000333188.3:n.*308_*309insTTTTTTTTTTA
NM_023067.3:c.*308_*309insTTTTTTTTTTA NP_075555.1:n.*308_*309insTTTTTTTTTTA
NM_023067.4:c.*308_*309insTTTTTTTTTTA MANE Select NP_075555.1:n.*308_*309insTTTTTTTTTTA