Canonical Allele Identifier: CA1405402311
Gene: FOXL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946036_138946048delinsAGCTGCTGCAGCC , CM000665.2:g.138946036_138946048delinsAGCTGCTGCAGCC GRCh38
NC_000003.11:g.138664878_138664890delinsAGCTGCTGCAGCC , CM000665.1:g.138664878_138664890delinsAGCTGCTGCAGCC GRCh37
NC_000003.10:g.140147568_140147580delinsAGCTGCTGCAGCC NCBI36
NG_012454.1:g.6093_6105delinsGGCTGCAGCAGCT
NG_029796.1:g.3803_3815delinsAGCTGCTGCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.675_687delinsGGCTGCAGCAGCT MANE Select ENSP00000497217.1:p.Ala225=
ENST00000330315.3:c.675_687delinsGGCTGCAGCAGCT ENSP00000333188.3:p.Ala225=
NM_023067.3:c.675_687delinsGGCTGCAGCAGCT NP_075555.1:p.Ala225=
NM_023067.4:c.675_687delinsGGCTGCAGCAGCT MANE Select NP_075555.1:p.Ala225=
Search 100 bp 5'
Search 100 bp 3'