Canonical Allele Identifier: CA2667924667
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945269_138945270insAGGA , CM000665.2:g.138945269_138945270insAGGA GRCh38
NC_000003.11:g.138664111_138664112insAGGA , CM000665.1:g.138664111_138664112insAGGA GRCh37
NC_000003.10:g.140146801_140146802insAGGA NCBI36
NG_012454.1:g.6871_6872insTCCT
NG_029796.1:g.3036_3037insAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*322_*323insTCCT MANE Select ENSP00000497217.1:n.*322_*323insTCCT
ENST00000330315.3:c.*322_*323insTCCT ENSP00000333188.3:n.*322_*323insTCCT
NM_023067.3:c.*322_*323insTCCT NP_075555.1:n.*322_*323insTCCT
NM_023067.4:c.*322_*323insTCCT MANE Select NP_075555.1:n.*322_*323insTCCT