Canonical Allele Identifier: CA2667924693
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945274_138945275del , CM000665.2:g.138945274_138945275del GRCh38
NC_000003.11:g.138664116_138664117del , CM000665.1:g.138664116_138664117del GRCh37
NC_000003.10:g.140146806_140146807del NCBI36
NG_012454.1:g.6866_6867del
NG_029796.1:g.3041_3042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*317_*318del MANE Select ENSP00000497217.1:n.*317_*318del
ENST00000330315.3:c.*317_*318del ENSP00000333188.3:n.*317_*318del
NM_023067.3:c.*317_*318del NP_075555.1:n.*317_*318del
NM_023067.4:c.*317_*318del MANE Select NP_075555.1:n.*317_*318del