Canonical Allele Identifier: CA2586973017
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945955_138945958del , CM000665.2:g.138945955_138945958del GRCh38
NC_000003.11:g.138664797_138664800del , CM000665.1:g.138664797_138664800del GRCh37
NC_000003.10:g.140147487_140147490del NCBI36
NG_012454.1:g.6184_6187del
NG_029796.1:g.3722_3725del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.766_769del MANE Select ENSP00000497217.1:p.Gly256ArgfsTer14
ENST00000330315.3:c.766_769del ENSP00000333188.3:p.Gly256ArgfsTer14
NM_023067.3:c.766_769del NP_075555.1:p.Gly256ArgfsTer14
NM_023067.4:c.766_769del MANE Select NP_075555.1:p.Gly256ArgfsTer14
Search 100 bp 5'
Search 100 bp 3'