Canonical Allele Identifier: CA1405402345
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946104_138946105delinsGT , CM000665.2:g.138946104_138946105delinsGT GRCh38
NC_000003.11:g.138664946_138664947delinsGT , CM000665.1:g.138664946_138664947delinsGT GRCh37
NC_000003.10:g.140147636_140147637delinsGT NCBI36
NG_012454.1:g.6036_6037delinsAC
NG_029796.1:g.3871_3872delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.618_619delinsAC MANE Select ENSP00000497217.1:p.Leu206=
ENST00000330315.3:c.618_619delinsAC ENSP00000333188.3:p.Leu206=
NM_023067.3:c.618_619delinsAC NP_075555.1:p.Leu206=
NM_023067.4:c.618_619delinsAC MANE Select NP_075555.1:p.Leu206=
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