Canonical Allele Identifier: CA2667925290
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945791-T-TGCGGTGGGGCAGGCG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945798_138945812dup , CM000665.2:g.138945798_138945812dup GRCh38
NC_000003.11:g.138664640_138664654dup , CM000665.1:g.138664640_138664654dup GRCh37
NC_000003.10:g.140147330_140147344dup NCBI36
NG_012454.1:g.6335_6349dup
NG_029796.1:g.3565_3579dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.917_931dup MANE Select ENSP00000497217.1:p.Pro310_His311insProProAlaProPro
ENST00000330315.3:c.917_931dup ENSP00000333188.3:p.Pro310_His311insProProAlaProPro
NM_023067.3:c.917_931dup NP_075555.1:p.Pro310_His311insProProAlaProPro
NM_023067.4:c.917_931dup MANE Select NP_075555.1:p.Pro310_His311insProProAlaProPro
Search 100 bp 5'
Search 100 bp 3'