Canonical Allele Identifier: CA1405402305
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946030_138946054delinsAGCCGCAGCTGCTGCAGCCGCTGCG , CM000665.2:g.138946030_138946054delinsAGCCGCAGCTGCTGCAGCCGCTGCG GRCh38
NC_000003.11:g.138664872_138664896delinsAGCCGCAGCTGCTGCAGCCGCTGCG , CM000665.1:g.138664872_138664896delinsAGCCGCAGCTGCTGCAGCCGCTGCG GRCh37
NC_000003.10:g.140147562_140147586delinsAGCCGCAGCTGCTGCAGCCGCTGCG NCBI36
NG_012454.1:g.6087_6111delinsCGCAGCGGCTGCAGCAGCTGCGGCT
NG_029796.1:g.3797_3821delinsAGCCGCAGCTGCTGCAGCCGCTGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.669_693delinsCGCAGCGGCTGCAGCAGCTGCGGCT MANE Select ENSP00000497217.1:p.Ala223=
ENST00000330315.3:c.669_693delinsCGCAGCGGCTGCAGCAGCTGCGGCT ENSP00000333188.3:p.Ala223=
NM_023067.3:c.669_693delinsCGCAGCGGCTGCAGCAGCTGCGGCT NP_075555.1:p.Ala223=
NM_023067.4:c.669_693delinsCGCAGCGGCTGCAGCAGCTGCGGCT MANE Select NP_075555.1:p.Ala223=
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