Canonical Allele Identifier: CA2667924712

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945276-T-TAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945276_138945277insAAAAA , CM000665.2:g.138945276_138945277insAAAAA	GRCh38
NC_000003.11:g.138664118_138664119insAAAAA , CM000665.1:g.138664118_138664119insAAAAA	GRCh37
NC_000003.10:g.140146808_140146809insAAAAA	NCBI36
NG_012454.1:g.6864_6865insTTTTT
NG_029796.1:g.3043_3044insAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*315_*316insTTTTT MANE Select	ENSP00000497217.1:n.*315_*316insTTTTT
ENST00000330315.3:c.*315_*316insTTTTT	ENSP00000333188.3:n.*315_*316insTTTTT
NM_023067.3:c.*315_*316insTTTTT	NP_075555.1:n.*315_*316insTTTTT
NM_023067.4:c.*315_*316insTTTTT MANE Select	NP_075555.1:n.*315_*316insTTTTT