Canonical Allele Identifier: CA2586973013

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945850dup , CM000665.2:g.138945850dup	GRCh38
NC_000003.11:g.138664692dup , CM000665.1:g.138664692dup	GRCh37
NC_000003.10:g.140147382dup	NCBI36
NG_012454.1:g.6293dup
NG_029796.1:g.3617dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000648323.1:c.875dup MANE Select	ENSP00000497217.1:p.His293AlafsTer?
ENST00000330315.3:c.875dup	ENSP00000333188.3:p.His293AlafsTer?
NM_023067.3:c.875dup	NP_075555.1:p.His293AlafsTer?
NM_023067.4:c.875dup MANE Select	NP_075555.1:p.His293AlafsTer?