Canonical Allele Identifier: CA2667924656
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945266_138945273del , CM000665.2:g.138945266_138945273del GRCh38
NC_000003.11:g.138664108_138664115del , CM000665.1:g.138664108_138664115del GRCh37
NC_000003.10:g.140146798_140146805del NCBI36
NG_012454.1:g.6868_6875del
NG_029796.1:g.3033_3040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*319_*326del MANE Select ENSP00000497217.1:n.*319_*326del
ENST00000330315.3:c.*319_*326del ENSP00000333188.3:n.*319_*326del
NM_023067.3:c.*319_*326del NP_075555.1:n.*319_*326del
NM_023067.4:c.*319_*326del MANE Select NP_075555.1:n.*319_*326del