Canonical Allele Identifier: CA2667924714

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945277-T-TAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945277_138945278insAAAA , CM000665.2:g.138945277_138945278insAAAA	GRCh38
NC_000003.11:g.138664119_138664120insAAAA , CM000665.1:g.138664119_138664120insAAAA	GRCh37
NC_000003.10:g.140146809_140146810insAAAA	NCBI36
NG_012454.1:g.6863_6864insTTTT
NG_029796.1:g.3044_3045insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*314_*315insTTTT MANE Select	ENSP00000497217.1:n.*314_*315insTTTT
ENST00000330315.3:c.*314_*315insTTTT	ENSP00000333188.3:n.*314_*315insTTTT
NM_023067.3:c.*314_*315insTTTT	NP_075555.1:n.*314_*315insTTTT
NM_023067.4:c.*314_*315insTTTT MANE Select	NP_075555.1:n.*314_*315insTTTT