Canonical Allele Identifier: CA2704132283

Gene: FOXL2

Linked Data

• dbSNP Id: rs2107744985

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946597del , CM000665.2:g.138946597del	GRCh38
NC_000003.11:g.138665439del , CM000665.1:g.138665439del	GRCh37
NC_000003.10:g.140148129del	NCBI36
NG_012454.1:g.5544del
NG_029796.1:g.4364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.126del MANE Select	ENSP00000497217.1:p.Thr44GlnfsTer?
ENST00000330315.3:c.126del	ENSP00000333188.3:p.Thr44GlnfsTer?
NM_023067.3:c.126del	NP_075555.1:p.Thr44GlnfsTer?
NM_023067.4:c.126del MANE Select	NP_075555.1:p.Thr44GlnfsTer?