Canonical Allele Identifier: CA2667924684
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945272_138945273insCAGTAAA , CM000665.2:g.138945272_138945273insCAGTAAA GRCh38
NC_000003.11:g.138664114_138664115insCAGTAAA , CM000665.1:g.138664114_138664115insCAGTAAA GRCh37
NC_000003.10:g.140146804_140146805insCAGTAAA NCBI36
NG_012454.1:g.6868_6869insTTTACTG
NG_029796.1:g.3039_3040insCAGTAAA

Transcript Alleles

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