Canonical Allele Identifier: CA2577918194
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946027_138946029del , CM000665.2:g.138946027_138946029del GRCh38
NC_000003.11:g.138664869_138664871del , CM000665.1:g.138664869_138664871del GRCh37
NC_000003.10:g.140147559_140147561del NCBI36
NG_012454.1:g.6114_6116del
NG_029796.1:g.3794_3796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.696_698del MANE Select ENSP00000497217.1:p.Ala233del
ENST00000330315.3:c.696_698del ENSP00000333188.3:p.Ala233del
NM_023067.3:c.696_698del NP_075555.1:p.Ala233del
NM_023067.4:c.696_698del MANE Select NP_075555.1:p.Ala233del
Search 100 bp 5'
Search 100 bp 3'