Canonical Allele Identifier: CA2667924686
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945272-G-GTAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945272_138945273insTAA , CM000665.2:g.138945272_138945273insTAA GRCh38
NC_000003.11:g.138664114_138664115insTAA , CM000665.1:g.138664114_138664115insTAA GRCh37
NC_000003.10:g.140146804_140146805insTAA NCBI36
NG_012454.1:g.6868_6869insTTA
NG_029796.1:g.3039_3040insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*319_*320insTTA MANE Select ENSP00000497217.1:n.*319_*320insTTA
ENST00000330315.3:c.*319_*320insTTA ENSP00000333188.3:n.*319_*320insTTA
NM_023067.3:c.*319_*320insTTA NP_075555.1:n.*319_*320insTTA
NM_023067.4:c.*319_*320insTTA MANE Select NP_075555.1:n.*319_*320insTTA
Search 100 bp 5'
Search 100 bp 3'