Canonical Allele Identifier: CA2667924606
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945252-CCCCGGGCCCTTTCCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945254_138945268del , CM000665.2:g.138945254_138945268del GRCh38
NC_000003.11:g.138664096_138664110del , CM000665.1:g.138664096_138664110del GRCh37
NC_000003.10:g.140146786_140146800del NCBI36
NG_012454.1:g.6874_6888del
NG_029796.1:g.3021_3035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*325_*339del MANE Select ENSP00000497217.1:n.*325_*339del
ENST00000330315.3:c.*325_*339del ENSP00000333188.3:n.*325_*339del
NM_023067.3:c.*325_*339del NP_075555.1:n.*325_*339del
NM_023067.4:c.*325_*339del MANE Select NP_075555.1:n.*325_*339del
Search 100 bp 5'
Search 100 bp 3'