Canonical Allele Identifier: CA2667926182
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946039_138946047del , CM000665.2:g.138946039_138946047del GRCh38
NC_000003.11:g.138664881_138664889del , CM000665.1:g.138664881_138664889del GRCh37
NC_000003.10:g.140147571_140147579del NCBI36
NG_012454.1:g.6099_6107del
NG_029796.1:g.3806_3814del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.681_689del MANE Select ENSP00000497217.1:p.Ala228_Ala230del
ENST00000330315.3:c.681_689del ENSP00000333188.3:p.Ala228_Ala230del
NM_023067.3:c.681_689del NP_075555.1:p.Ala228_Ala230del
NM_023067.4:c.681_689del MANE Select NP_075555.1:p.Ala228_Ala230del