Canonical Allele Identifier: CA1405402082
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945395_138945397delinsCAT , CM000665.2:g.138945395_138945397delinsCAT GRCh38
NC_000003.11:g.138664237_138664239delinsCAT , CM000665.1:g.138664237_138664239delinsCAT GRCh37
NC_000003.10:g.140146927_140146929delinsCAT NCBI36
NG_012454.1:g.6744_6746delinsATG
NG_029796.1:g.3162_3164delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*195_*197delinsATG MANE Select ENSP00000497217.1:n.*195_*197delinsATG
ENST00000330315.3:c.*195_*197delinsATG ENSP00000333188.3:n.*195_*197delinsATG
NM_023067.3:c.*195_*197delinsATG NP_075555.1:n.*195_*197delinsATG
NM_023067.4:c.*195_*197delinsATG MANE Select NP_075555.1:n.*195_*197delinsATG