Canonical Allele Identifier: CA2667924708

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945276-TTGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945277_138945280del , CM000665.2:g.138945277_138945280del	GRCh38
NC_000003.11:g.138664119_138664122del , CM000665.1:g.138664119_138664122del	GRCh37
NC_000003.10:g.140146809_140146812del	NCBI36
NG_012454.1:g.6861_6864del
NG_029796.1:g.3044_3047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*312_*315del MANE Select	ENSP00000497217.1:n.*312_*315del
ENST00000330315.3:c.*312_*315del	ENSP00000333188.3:n.*312_*315del
NM_023067.3:c.*312_*315del	NP_075555.1:n.*312_*315del
NM_023067.4:c.*312_*315del MANE Select	NP_075555.1:n.*312_*315del