Canonical Allele Identifier: CA1405402289

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946019_138946046delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG , CM000665.2:g.138946019_138946046delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG	GRCh38
NC_000003.11:g.138664861_138664888delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG , CM000665.1:g.138664861_138664888delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG	GRCh37
NC_000003.10:g.140147551_140147578delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG	NCBI36
NG_012454.1:g.6095_6122delinsCTGCAGCAGCTGCGGCTGCAGCCGCGGG
NG_029796.1:g.3786_3813delinsCCCGCGGCTGCAGCCGCAGCTGCTGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.677_704delinsCTGCAGCAGCTGCGGCTGCAGCCGCGGG MANE Select	ENSP00000497217.1:p.Ala226=
ENST00000330315.3:c.677_704delinsCTGCAGCAGCTGCGGCTGCAGCCGCGGG	ENSP00000333188.3:p.Ala226=
NM_023067.3:c.677_704delinsCTGCAGCAGCTGCGGCTGCAGCCGCGGG	NP_075555.1:p.Ala226=
NM_023067.4:c.677_704delinsCTGCAGCAGCTGCGGCTGCAGCCGCGGG MANE Select	NP_075555.1:p.Ala226=