Canonical Allele Identifier: CA2667925455
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945847-CGGGTGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945853_138945858del , CM000665.2:g.138945853_138945858del GRCh38
NC_000003.11:g.138664695_138664700del , CM000665.1:g.138664695_138664700del GRCh37
NC_000003.10:g.140147385_140147390del NCBI36
NG_012454.1:g.6288_6293del
NG_029796.1:g.3620_3625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.870_875del MANE Select ENSP00000497217.1:p.His291_Pro292del
ENST00000330315.3:c.870_875del ENSP00000333188.3:p.His291_Pro292del
NM_023067.3:c.870_875del NP_075555.1:p.His291_Pro292del
NM_023067.4:c.870_875del MANE Select NP_075555.1:p.His291_Pro292del
Search 100 bp 5'
Search 100 bp 3'