Canonical Allele Identifier: CA2667924641

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945262-TTTCCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945263_138945267del , CM000665.2:g.138945263_138945267del	GRCh38
NC_000003.11:g.138664105_138664109del , CM000665.1:g.138664105_138664109del	GRCh37
NC_000003.10:g.140146795_140146799del	NCBI36
NG_012454.1:g.6874_6878del
NG_029796.1:g.3030_3034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*325_*329del MANE Select	ENSP00000497217.1:n.*325_*329del
ENST00000330315.3:c.*325_*329del	ENSP00000333188.3:n.*325_*329del
NM_023067.3:c.*325_*329del	NP_075555.1:n.*325_*329del
NM_023067.4:c.*325_*329del MANE Select	NP_075555.1:n.*325_*329del