Canonical Allele Identifier: CA2667924690

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945272-G-GCATAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945272_138945273insCATAAAAA , CM000665.2:g.138945272_138945273insCATAAAAA	GRCh38
NC_000003.11:g.138664114_138664115insCATAAAAA , CM000665.1:g.138664114_138664115insCATAAAAA	GRCh37
NC_000003.10:g.140146804_140146805insCATAAAAA	NCBI36
NG_012454.1:g.6868_6869insTTTTTATG
NG_029796.1:g.3039_3040insCATAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*319_*320insTTTTTATG MANE Select	ENSP00000497217.1:n.*319_*320insTTTTTATG
ENST00000330315.3:c.*319_*320insTTTTTATG	ENSP00000333188.3:n.*319_*320insTTTTTATG
NM_023067.3:c.*319_*320insTTTTTATG	NP_075555.1:n.*319_*320insTTTTTATG
NM_023067.4:c.*319_*320insTTTTTATG MANE Select	NP_075555.1:n.*319_*320insTTTTTATG