Canonical Allele Identifier: CA2667924687
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945272_138945273insTAAAA , CM000665.2:g.138945272_138945273insTAAAA GRCh38
NC_000003.11:g.138664114_138664115insTAAAA , CM000665.1:g.138664114_138664115insTAAAA GRCh37
NC_000003.10:g.140146804_140146805insTAAAA NCBI36
NG_012454.1:g.6868_6869insTTTTA
NG_029796.1:g.3039_3040insTAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*319_*320insTTTTA MANE Select ENSP00000497217.1:n.*319_*320insTTTTA
ENST00000330315.3:c.*319_*320insTTTTA ENSP00000333188.3:n.*319_*320insTTTTA
NM_023067.3:c.*319_*320insTTTTA NP_075555.1:n.*319_*320insTTTTA
NM_023067.4:c.*319_*320insTTTTA MANE Select NP_075555.1:n.*319_*320insTTTTA