Canonical Allele Identifier: CA2667924688
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945273_138945274insTTAAAAA , CM000665.2:g.138945273_138945274insTTAAAAA GRCh38
NC_000003.11:g.138664115_138664116insTTAAAAA , CM000665.1:g.138664115_138664116insTTAAAAA GRCh37
NC_000003.10:g.140146805_140146806insTTAAAAA NCBI36
NG_012454.1:g.6868_6869insTTTTAAT
NG_029796.1:g.3040_3041insTTAAAAA

Transcript Alleles

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