Canonical Allele Identifier: CA1405402472

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946339C= , CM000665.2:g.138946339C=	GRCh38
NC_000003.11:g.138665181C= , CM000665.1:g.138665181C=	GRCh37
NC_000003.10:g.140147871C=	NCBI36
NG_012454.1:g.5802G=
NG_029796.1:g.4106C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000648323.1:c.384G= MANE Select	ENSP00000497217.1:p.Trp128=
ENST00000330315.3:c.384G=	ENSP00000333188.3:p.Trp128=
NM_023067.3:c.384G=	NP_075555.1:p.Trp128=
NM_023067.4:c.384G= MANE Select	NP_075555.1:p.Trp128=