Canonical Allele Identifier: CA1405402489
Gene: FOXL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946384_138946385delinsGA , CM000665.2:g.138946384_138946385delinsGA GRCh38
NC_000003.11:g.138665226_138665227delinsGA , CM000665.1:g.138665226_138665227delinsGA GRCh37
NC_000003.10:g.140147916_140147917delinsGA NCBI36
NG_012454.1:g.5756_5757delinsTC
NG_029796.1:g.4151_4152delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.338_339delinsTC MANE Select ENSP00000497217.1:p.Ile113=
ENST00000330315.3:c.338_339delinsTC ENSP00000333188.3:p.Ile113=
NM_023067.3:c.338_339delinsTC NP_075555.1:p.Ile113=
NM_023067.4:c.338_339delinsTC MANE Select NP_075555.1:p.Ile113=
Search 100 bp 5'
Search 100 bp 3'