Canonical Allele Identifier: CA2667924716
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945278_138945280del , CM000665.2:g.138945278_138945280del GRCh38
NC_000003.11:g.138664120_138664122del , CM000665.1:g.138664120_138664122del GRCh37
NC_000003.10:g.140146810_140146812del NCBI36
NG_012454.1:g.6861_6863del
NG_029796.1:g.3045_3047del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*312_*314del MANE Select ENSP00000497217.1:n.*312_*314del
ENST00000330315.3:c.*312_*314del ENSP00000333188.3:n.*312_*314del
NM_023067.3:c.*312_*314del NP_075555.1:n.*312_*314del
NM_023067.4:c.*312_*314del MANE Select NP_075555.1:n.*312_*314del