Canonical Allele Identifier: CA2667924722

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945279-GGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945280_138945281del , CM000665.2:g.138945280_138945281del	GRCh38
NC_000003.11:g.138664122_138664123del , CM000665.1:g.138664122_138664123del	GRCh37
NC_000003.10:g.140146812_140146813del	NCBI36
NG_012454.1:g.6860_6861del
NG_029796.1:g.3047_3048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*311_*312del MANE Select	ENSP00000497217.1:n.*311_*312del
ENST00000330315.3:c.*311_*312del	ENSP00000333188.3:n.*311_*312del
NM_023067.3:c.*311_*312del	NP_075555.1:n.*311_*312del
NM_023067.4:c.*311_*312del MANE Select	NP_075555.1:n.*311_*312del