Canonical Allele Identifier: CA1405402306
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946030_138946039delinsAGCCGCAGCT , CM000665.2:g.138946030_138946039delinsAGCCGCAGCT GRCh38
NC_000003.11:g.138664872_138664881delinsAGCCGCAGCT , CM000665.1:g.138664872_138664881delinsAGCCGCAGCT GRCh37
NC_000003.10:g.140147562_140147571delinsAGCCGCAGCT NCBI36
NG_012454.1:g.6102_6111delinsAGCTGCGGCT
NG_029796.1:g.3797_3806delinsAGCCGCAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.684_693delinsAGCTGCGGCT MANE Select ENSP00000497217.1:p.Ala228=
ENST00000330315.3:c.684_693delinsAGCTGCGGCT ENSP00000333188.3:p.Ala228=
NM_023067.3:c.684_693delinsAGCTGCGGCT NP_075555.1:p.Ala228=
NM_023067.4:c.684_693delinsAGCTGCGGCT MANE Select NP_075555.1:p.Ala228=
Search 100 bp 5'
Search 100 bp 3'