Canonical Allele Identifier: CA2667924662
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945268del , CM000665.2:g.138945268del GRCh38
NC_000003.11:g.138664110del , CM000665.1:g.138664110del GRCh37
NC_000003.10:g.140146800del NCBI36
NG_012454.1:g.6873del
NG_029796.1:g.3035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*324del MANE Select ENSP00000497217.1:n.*324del
ENST00000330315.3:c.*324del ENSP00000333188.3:n.*324del
NM_023067.3:c.*324del NP_075555.1:n.*324del
NM_023067.4:c.*324del MANE Select NP_075555.1:n.*324del