Canonical Allele Identifier: CA2667924713

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945276-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945276_138945277insAAA , CM000665.2:g.138945276_138945277insAAA	GRCh38
NC_000003.11:g.138664118_138664119insAAA , CM000665.1:g.138664118_138664119insAAA	GRCh37
NC_000003.10:g.140146808_140146809insAAA	NCBI36
NG_012454.1:g.6864_6865insTTT
NG_029796.1:g.3043_3044insAAA

Transcript Alleles

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