Canonical Allele Identifier: CA917019803

Gene: FOXL2

Linked Data

• dbSNP Id: rs1559921440
• gnomAD v4: 3-138945329-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945334_138945335del , CM000665.2:g.138945334_138945335del	GRCh38
NC_000003.11:g.138664176_138664177del , CM000665.1:g.138664176_138664177del	GRCh37
NC_000003.10:g.140146866_140146867del	NCBI36
NG_012454.1:g.6810_6811del
NG_029796.1:g.3101_3102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*261_*262del MANE Select	ENSP00000497217.1:n.*261_*262del
ENST00000330315.3:c.*261_*262del	ENSP00000333188.3:n.*261_*262del
NM_023067.3:c.*261_*262del	NP_075555.1:n.*261_*262del
NM_023067.4:c.*261_*262del MANE Select	NP_075555.1:n.*261_*262del