Canonical Allele Identifier: CA2758614461
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946035_138946039del , CM000665.2:g.138946035_138946039del GRCh38
NC_000003.11:g.138664877_138664881del , CM000665.1:g.138664877_138664881del GRCh37
NC_000003.10:g.140147567_140147571del NCBI36
NG_012454.1:g.6102_6106del
NG_029796.1:g.3802_3806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.684_688del MANE Select ENSP00000497217.1:p.Ala229GlyfsTer8
ENST00000330315.3:c.684_688del ENSP00000333188.3:p.Ala229GlyfsTer8
NM_023067.3:c.684_688del NP_075555.1:p.Ala229GlyfsTer8
NM_023067.4:c.684_688del MANE Select NP_075555.1:p.Ala229GlyfsTer8
Search 100 bp 5'
Search 100 bp 3'