Canonical Allele Identifier: CA1405401759

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945460_138945461delinsTG , CM000665.2:g.138945460_138945461delinsTG	GRCh38
NC_000003.11:g.138664302_138664303delinsTG , CM000665.1:g.138664302_138664303delinsTG	GRCh37
NC_000003.10:g.140146992_140146993delinsTG	NCBI36
NG_012454.1:g.6680_6681delinsCA
NG_029796.1:g.3227_3228delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*131_*132delinsCA MANE Select	ENSP00000497217.1:n.*131_*132delinsCA
ENST00000330315.3:c.*131_*132delinsCA	ENSP00000333188.3:n.*131_*132delinsCA
NM_023067.3:c.*131_*132delinsCA	NP_075555.1:n.*131_*132delinsCA
NM_023067.4:c.*131_*132delinsCA MANE Select	NP_075555.1:n.*131_*132delinsCA