Canonical Allele Identifier: CA2667924889
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945392_138945394del , CM000665.2:g.138945392_138945394del GRCh38
NC_000003.11:g.138664234_138664236del , CM000665.1:g.138664234_138664236del GRCh37
NC_000003.10:g.140146924_140146926del NCBI36
NG_012454.1:g.6751_6753del
NG_029796.1:g.3159_3161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*202_*204del MANE Select ENSP00000497217.1:n.*202_*204del
ENST00000330315.3:c.*202_*204del ENSP00000333188.3:n.*202_*204del
NM_023067.3:c.*202_*204del NP_075555.1:n.*202_*204del
NM_023067.4:c.*202_*204del MANE Select NP_075555.1:n.*202_*204del