Canonical Allele Identifier: CA1405402321
Gene: FOXL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946048_138946051delinsCGCT , CM000665.2:g.138946048_138946051delinsCGCT GRCh38
NC_000003.11:g.138664890_138664893delinsCGCT , CM000665.1:g.138664890_138664893delinsCGCT GRCh37
NC_000003.10:g.140147580_140147583delinsCGCT NCBI36
NG_012454.1:g.6090_6093delinsAGCG
NG_029796.1:g.3815_3818delinsCGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.672_675delinsAGCG MANE Select ENSP00000497217.1:p.Ala224=
ENST00000330315.3:c.672_675delinsAGCG ENSP00000333188.3:p.Ala224=
NM_023067.3:c.672_675delinsAGCG NP_075555.1:p.Ala224=
NM_023067.4:c.672_675delinsAGCG MANE Select NP_075555.1:p.Ala224=
Search 100 bp 5'
Search 100 bp 3'