Canonical Allele Identifier: CA2667924679
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945271_138945272insCTCATTAAA , CM000665.2:g.138945271_138945272insCTCATTAAA GRCh38
NC_000003.11:g.138664113_138664114insCTCATTAAA , CM000665.1:g.138664113_138664114insCTCATTAAA GRCh37
NC_000003.10:g.140146803_140146804insCTCATTAAA NCBI36
NG_012454.1:g.6869_6870insTTTAATGAG
NG_029796.1:g.3038_3039insCTCATTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*320_*321insTTTAATGAG MANE Select ENSP00000497217.1:n.*320_*321insTTTAATGAG
ENST00000330315.3:c.*320_*321insTTTAATGAG ENSP00000333188.3:n.*320_*321insTTTAATGAG
NM_023067.3:c.*320_*321insTTTAATGAG NP_075555.1:n.*320_*321insTTTAATGAG
NM_023067.4:c.*320_*321insTTTAATGAG MANE Select NP_075555.1:n.*320_*321insTTTAATGAG