Canonical Allele Identifier: CA913102158
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138946030-AGCCGCAGCTGCTGCAGCC-A
MyVariant Identifiers: chr3:g.138664873_138664890del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946033_138946050del , CM000665.2:g.138946033_138946050del GRCh38
NC_000003.11:g.138664875_138664892del , CM000665.1:g.138664875_138664892del GRCh37
NC_000003.10:g.140147565_140147582del NCBI36
NG_012454.1:g.6093_6110del
NG_029796.1:g.3800_3817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.675_692del MANE Select ENSP00000497217.1:p.Ala226_Ala231del
ENST00000330315.3:c.675_692del ENSP00000333188.3:p.Ala226_Ala231del
NM_023067.3:c.675_692del NP_075555.1:p.Ala226_Ala231del
NM_023067.4:c.675_692del MANE Select NP_075555.1:p.Ala226_Ala231del
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