Canonical Allele Identifier: CA354700704
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945668T>G , CM000665.2:g.138945668T>G GRCh38
NC_000003.11:g.138664510T>G , CM000665.1:g.138664510T>G GRCh37
NC_000003.10:g.140147200T>G NCBI36
NG_012454.1:g.6473A>C
NG_029796.1:g.3435T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.1055A>C MANE Select ENSP00000497217.1:p.Glu352Ala
ENST00000330315.3:c.1055A>C ENSP00000333188.3:p.Glu352Ala
NM_023067.3:c.1055A>C NP_075555.1:p.Glu352Ala
NM_023067.4:c.1055A>C MANE Select NP_075555.1:p.Glu352Ala