Canonical Allele Identifier: CA2667924694
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945274-ATT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945276_138945277del , CM000665.2:g.138945276_138945277del GRCh38
NC_000003.11:g.138664118_138664119del , CM000665.1:g.138664118_138664119del GRCh37
NC_000003.10:g.140146808_140146809del NCBI36
NG_012454.1:g.6865_6866del
NG_029796.1:g.3043_3044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*316_*317del MANE Select ENSP00000497217.1:n.*316_*317del
ENST00000330315.3:c.*316_*317del ENSP00000333188.3:n.*316_*317del
NM_023067.3:c.*316_*317del NP_075555.1:n.*316_*317del
NM_023067.4:c.*316_*317del MANE Select NP_075555.1:n.*316_*317del
Search 100 bp 5'
Search 100 bp 3'