Canonical Allele Identifier: CA2667924646

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945263-TTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945264_138945266del , CM000665.2:g.138945264_138945266del	GRCh38
NC_000003.11:g.138664106_138664108del , CM000665.1:g.138664106_138664108del	GRCh37
NC_000003.10:g.140146796_140146798del	NCBI36
NG_012454.1:g.6875_6877del
NG_029796.1:g.3031_3033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*326_*328del MANE Select	ENSP00000497217.1:n.*326_*328del
ENST00000330315.3:c.*326_*328del	ENSP00000333188.3:n.*326_*328del
NM_023067.3:c.*326_*328del	NP_075555.1:n.*326_*328del
NM_023067.4:c.*326_*328del MANE Select	NP_075555.1:n.*326_*328del