Canonical Allele Identifier: CA2667924701

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945275-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945275_138945276insCA , CM000665.2:g.138945275_138945276insCA	GRCh38
NC_000003.11:g.138664117_138664118insCA , CM000665.1:g.138664117_138664118insCA	GRCh37
NC_000003.10:g.140146807_140146808insCA	NCBI36
NG_012454.1:g.6865_6866insTG
NG_029796.1:g.3042_3043insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*316_*317insTG MANE Select	ENSP00000497217.1:n.*316_*317insTG
ENST00000330315.3:c.*316_*317insTG	ENSP00000333188.3:n.*316_*317insTG
NM_023067.3:c.*316_*317insTG	NP_075555.1:n.*316_*317insTG
NM_023067.4:c.*316_*317insTG MANE Select	NP_075555.1:n.*316_*317insTG