Canonical Allele Identifier: CA2667924640
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945263_138945265del , CM000665.2:g.138945263_138945265del GRCh38
NC_000003.11:g.138664105_138664107del , CM000665.1:g.138664105_138664107del GRCh37
NC_000003.10:g.140146795_140146797del NCBI36
NG_012454.1:g.6876_6878del
NG_029796.1:g.3030_3032del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*327_*329del MANE Select ENSP00000497217.1:n.*327_*329del
ENST00000330315.3:c.*327_*329del ENSP00000333188.3:n.*327_*329del
NM_023067.3:c.*327_*329del NP_075555.1:n.*327_*329del
NM_023067.4:c.*327_*329del MANE Select NP_075555.1:n.*327_*329del