Canonical Allele Identifier: CA2667925218
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945769_138945770del , CM000665.2:g.138945769_138945770del GRCh38
NC_000003.11:g.138664611_138664612del , CM000665.1:g.138664611_138664612del GRCh37
NC_000003.10:g.140147301_140147302del NCBI36
NG_012454.1:g.6372_6373del
NG_029796.1:g.3536_3537del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.954_955del MANE Select ENSP00000497217.1:p.Pro319GlyfsTer?
ENST00000330315.3:c.954_955del ENSP00000333188.3:p.Pro319GlyfsTer?
NM_023067.3:c.954_955del NP_075555.1:p.Pro319GlyfsTer?
NM_023067.4:c.954_955del MANE Select NP_075555.1:p.Pro319GlyfsTer?