Canonical Allele Identifier: CA1405402296
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946024_138946048delinsGGCTGCAGCCGCAGCTGCTGCAGCC , CM000665.2:g.138946024_138946048delinsGGCTGCAGCCGCAGCTGCTGCAGCC GRCh38
NC_000003.11:g.138664866_138664890delinsGGCTGCAGCCGCAGCTGCTGCAGCC , CM000665.1:g.138664866_138664890delinsGGCTGCAGCCGCAGCTGCTGCAGCC GRCh37
NC_000003.10:g.140147556_140147580delinsGGCTGCAGCCGCAGCTGCTGCAGCC NCBI36
NG_012454.1:g.6093_6117delinsGGCTGCAGCAGCTGCGGCTGCAGCC
NG_029796.1:g.3791_3815delinsGGCTGCAGCCGCAGCTGCTGCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.675_699delinsGGCTGCAGCAGCTGCGGCTGCAGCC MANE Select ENSP00000497217.1:p.Ala225=
ENST00000330315.3:c.675_699delinsGGCTGCAGCAGCTGCGGCTGCAGCC ENSP00000333188.3:p.Ala225=
NM_023067.3:c.675_699delinsGGCTGCAGCAGCTGCGGCTGCAGCC NP_075555.1:p.Ala225=
NM_023067.4:c.675_699delinsGGCTGCAGCAGCTGCGGCTGCAGCC MANE Select NP_075555.1:p.Ala225=
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