Canonical Allele Identifier: CA2667924671

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945270-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945271_138945272insCT , CM000665.2:g.138945271_138945272insCT	GRCh38
NC_000003.11:g.138664113_138664114insCT , CM000665.1:g.138664113_138664114insCT	GRCh37
NC_000003.10:g.140146803_140146804insCT	NCBI36
NG_012454.1:g.6870_6871insGA
NG_029796.1:g.3038_3039insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*321_*322insGA MANE Select	ENSP00000497217.1:n.*321_*322insGA
ENST00000330315.3:c.*321_*322insGA	ENSP00000333188.3:n.*321_*322insGA
NM_023067.3:c.*321_*322insGA	NP_075555.1:n.*321_*322insGA
NM_023067.4:c.*321_*322insGA MANE Select	NP_075555.1:n.*321_*322insGA