Canonical Allele Identifier: CA2667924707
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945277_138945284del , CM000665.2:g.138945277_138945284del GRCh38
NC_000003.11:g.138664119_138664126del , CM000665.1:g.138664119_138664126del GRCh37
NC_000003.10:g.140146809_140146816del NCBI36
NG_012454.1:g.6857_6864del
NG_029796.1:g.3044_3051del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*308_*315del MANE Select ENSP00000497217.1:n.*308_*315del
ENST00000330315.3:c.*308_*315del ENSP00000333188.3:n.*308_*315del
NM_023067.3:c.*308_*315del NP_075555.1:n.*308_*315del
NM_023067.4:c.*308_*315del MANE Select NP_075555.1:n.*308_*315del