Canonical Allele Identifier: CA2667924675
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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