Canonical Allele Identifier: CA2667924689
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945272_138945273insCAGTAAAA , CM000665.2:g.138945272_138945273insCAGTAAAA GRCh38
NC_000003.11:g.138664114_138664115insCAGTAAAA , CM000665.1:g.138664114_138664115insCAGTAAAA GRCh37
NC_000003.10:g.140146804_140146805insCAGTAAAA NCBI36
NG_012454.1:g.6868_6869insTTTTACTG
NG_029796.1:g.3039_3040insCAGTAAAA

Transcript Alleles

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