Canonical Allele Identifier: CA2586973024
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946018dup , CM000665.2:g.138946018dup GRCh38
NC_000003.11:g.138664860dup , CM000665.1:g.138664860dup GRCh37
NC_000003.10:g.140147550dup NCBI36
NG_012454.1:g.6126dup
NG_029796.1:g.3785dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.708dup MANE Select ENSP00000497217.1:p.Gly237ArgfsTer2
ENST00000330315.3:c.708dup ENSP00000333188.3:p.Gly237ArgfsTer2
NM_023067.3:c.708dup NP_075555.1:p.Gly237ArgfsTer2
NM_023067.4:c.708dup MANE Select NP_075555.1:p.Gly237ArgfsTer2
Search 100 bp 5'
Search 100 bp 3'