Canonical Allele Identifier: CA1405402292
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946021_138946045delinsCGCGGCTGCAGCCGCAGCTGCTGCA , CM000665.2:g.138946021_138946045delinsCGCGGCTGCAGCCGCAGCTGCTGCA GRCh38
NC_000003.11:g.138664863_138664887delinsCGCGGCTGCAGCCGCAGCTGCTGCA , CM000665.1:g.138664863_138664887delinsCGCGGCTGCAGCCGCAGCTGCTGCA GRCh37
NC_000003.10:g.140147553_140147577delinsCGCGGCTGCAGCCGCAGCTGCTGCA NCBI36
NG_012454.1:g.6096_6120delinsTGCAGCAGCTGCGGCTGCAGCCGCG
NG_029796.1:g.3788_3812delinsCGCGGCTGCAGCCGCAGCTGCTGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.678_702delinsTGCAGCAGCTGCGGCTGCAGCCGCG MANE Select ENSP00000497217.1:p.Ala226=
ENST00000330315.3:c.678_702delinsTGCAGCAGCTGCGGCTGCAGCCGCG ENSP00000333188.3:p.Ala226=
NM_023067.3:c.678_702delinsTGCAGCAGCTGCGGCTGCAGCCGCG NP_075555.1:p.Ala226=
NM_023067.4:c.678_702delinsTGCAGCAGCTGCGGCTGCAGCCGCG MANE Select NP_075555.1:p.Ala226=