Canonical Allele Identifier: CA2667924699
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945275_138945277del , CM000665.2:g.138945275_138945277del GRCh38
NC_000003.11:g.138664117_138664119del , CM000665.1:g.138664117_138664119del GRCh37
NC_000003.10:g.140146807_140146809del NCBI36
NG_012454.1:g.6864_6866del
NG_029796.1:g.3042_3044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*315_*317del MANE Select ENSP00000497217.1:n.*315_*317del
ENST00000330315.3:c.*315_*317del ENSP00000333188.3:n.*315_*317del
NM_023067.3:c.*315_*317del NP_075555.1:n.*315_*317del
NM_023067.4:c.*315_*317del MANE Select NP_075555.1:n.*315_*317del