Canonical Allele Identifier: CA2667924674
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945271_138945273del , CM000665.2:g.138945271_138945273del GRCh38
NC_000003.11:g.138664113_138664115del , CM000665.1:g.138664113_138664115del GRCh37
NC_000003.10:g.140146803_140146805del NCBI36
NG_012454.1:g.6868_6870del
NG_029796.1:g.3038_3040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*319_*321del MANE Select ENSP00000497217.1:n.*319_*321del
ENST00000330315.3:c.*319_*321del ENSP00000333188.3:n.*319_*321del
NM_023067.3:c.*319_*321del NP_075555.1:n.*319_*321del
NM_023067.4:c.*319_*321del MANE Select NP_075555.1:n.*319_*321del