Canonical Allele Identifier: CA2667924624
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945258_138945260del , CM000665.2:g.138945258_138945260del GRCh38
NC_000003.11:g.138664100_138664102del , CM000665.1:g.138664100_138664102del GRCh37
NC_000003.10:g.140146790_140146792del NCBI36
NG_012454.1:g.6881_6883del
NG_029796.1:g.3025_3027del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*332_*334del MANE Select ENSP00000497217.1:n.*332_*334del
ENST00000330315.3:c.*332_*334del ENSP00000333188.3:n.*332_*334del
NM_023067.3:c.*332_*334del NP_075555.1:n.*332_*334del
NM_023067.4:c.*332_*334del MANE Select NP_075555.1:n.*332_*334del