Canonical Allele Identifier: CA2667924657

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945265-CCGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945266_138945269del , CM000665.2:g.138945266_138945269del	GRCh38
NC_000003.11:g.138664108_138664111del , CM000665.1:g.138664108_138664111del	GRCh37
NC_000003.10:g.140146798_140146801del	NCBI36
NG_012454.1:g.6872_6875del
NG_029796.1:g.3033_3036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*323_*326del MANE Select	ENSP00000497217.1:n.*323_*326del
ENST00000330315.3:c.*323_*326del	ENSP00000333188.3:n.*323_*326del
NM_023067.3:c.*323_*326del	NP_075555.1:n.*323_*326del
NM_023067.4:c.*323_*326del MANE Select	NP_075555.1:n.*323_*326del