Canonical Allele Identifier: CA2667924633

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945260-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945261_138945263del , CM000665.2:g.138945261_138945263del	GRCh38
NC_000003.11:g.138664103_138664105del , CM000665.1:g.138664103_138664105del	GRCh37
NC_000003.10:g.140146793_140146795del	NCBI36
NG_012454.1:g.6878_6880del
NG_029796.1:g.3028_3030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*329_*331del MANE Select	ENSP00000497217.1:n.*329_*331del
ENST00000330315.3:c.*329_*331del	ENSP00000333188.3:n.*329_*331del
NM_023067.3:c.*329_*331del	NP_075555.1:n.*329_*331del
NM_023067.4:c.*329_*331del MANE Select	NP_075555.1:n.*329_*331del