Canonical Allele Identifier: CA2667924639
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945261-CTTT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945262_138945264del , CM000665.2:g.138945262_138945264del GRCh38
NC_000003.11:g.138664104_138664106del , CM000665.1:g.138664104_138664106del GRCh37
NC_000003.10:g.140146794_140146796del NCBI36
NG_012454.1:g.6877_6879del
NG_029796.1:g.3029_3031del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*328_*330del MANE Select ENSP00000497217.1:n.*328_*330del
ENST00000330315.3:c.*328_*330del ENSP00000333188.3:n.*328_*330del
NM_023067.3:c.*328_*330del NP_075555.1:n.*328_*330del
NM_023067.4:c.*328_*330del MANE Select NP_075555.1:n.*328_*330del
Search 100 bp 5'
Search 100 bp 3'