Canonical Allele Identifier: CA354700705
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945669C>A , CM000665.2:g.138945669C>A GRCh38
NC_000003.11:g.138664511C>A , CM000665.1:g.138664511C>A GRCh37
NC_000003.10:g.140147201C>A NCBI36
NG_012454.1:g.6472G>T
NG_029796.1:g.3436C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.1054G>T MANE Select ENSP00000497217.1:p.Glu352Ter
ENST00000330315.3:c.1054G>T ENSP00000333188.3:p.Glu352Ter
NM_023067.3:c.1054G>T NP_075555.1:p.Glu352Ter
NM_023067.4:c.1054G>T MANE Select NP_075555.1:p.Glu352Ter