Canonical Allele Identifier: CA2559492927
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946627_138946628insAGC , CM000665.2:g.138946627_138946628insAGC GRCh38
NC_000003.11:g.138665469_138665470insAGC , CM000665.1:g.138665469_138665470insAGC GRCh37
NC_000003.10:g.140148159_140148160insAGC NCBI36
NG_012454.1:g.5514_5515insCTG
NG_029796.1:g.4394_4395insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.96_97insCTG MANE Select ENSP00000497217.1:p.Pro32_Ser33insLeu
ENST00000330315.3:c.96_97insCTG ENSP00000333188.3:p.Pro32_Ser33insLeu
NM_023067.3:c.96_97insCTG NP_075555.1:p.Pro32_Ser33insLeu
NM_023067.4:c.96_97insCTG MANE Select NP_075555.1:p.Pro32_Ser33insLeu
Search 100 bp 5'
Search 100 bp 3'