Canonical Allele Identifier: CA2667924691

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945273-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945273_138945274insTC , CM000665.2:g.138945273_138945274insTC	GRCh38
NC_000003.11:g.138664115_138664116insTC , CM000665.1:g.138664115_138664116insTC	GRCh37
NC_000003.10:g.140146805_140146806insTC	NCBI36
NG_012454.1:g.6867_6868insGA
NG_029796.1:g.3040_3041insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*318_*319insGA MANE Select	ENSP00000497217.1:n.*318_*319insGA
ENST00000330315.3:c.*318_*319insGA	ENSP00000333188.3:n.*318_*319insGA
NM_023067.3:c.*318_*319insGA	NP_075555.1:n.*318_*319insGA
NM_023067.4:c.*318_*319insGA MANE Select	NP_075555.1:n.*318_*319insGA