Canonical Allele Identifier: CA2697556888
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2709291
ClinVar RCV Id: RCV003547929
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945702_138945705dup , CM000665.2:g.138945702_138945705dup GRCh38
NC_000003.11:g.138664544_138664547dup , CM000665.1:g.138664544_138664547dup GRCh37
NC_000003.10:g.140147234_140147237dup NCBI36
NG_012454.1:g.6436_6439dup
NG_029796.1:g.3469_3472dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1018_1021dup MANE Select ENSP00000497217.1:p.Pro341ArgfsTer?
ENST00000330315.3:c.1018_1021dup ENSP00000333188.3:p.Pro341ArgfsTer?
NM_023067.3:c.1018_1021dup NP_075555.1:p.Pro341ArgfsTer?
NM_023067.4:c.1018_1021dup MANE Select NP_075555.1:p.Pro341ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'