Canonical Allele Identifier: CA2667924642

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945262-TTTCCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945263_138945268del , CM000665.2:g.138945263_138945268del	GRCh38
NC_000003.11:g.138664105_138664110del , CM000665.1:g.138664105_138664110del	GRCh37
NC_000003.10:g.140146795_140146800del	NCBI36
NG_012454.1:g.6873_6878del
NG_029796.1:g.3030_3035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*324_*329del MANE Select	ENSP00000497217.1:n.*324_*329del
ENST00000330315.3:c.*324_*329del	ENSP00000333188.3:n.*324_*329del
NM_023067.3:c.*324_*329del	NP_075555.1:n.*324_*329del
NM_023067.4:c.*324_*329del MANE Select	NP_075555.1:n.*324_*329del