Canonical Allele Identifier: CA2667925120
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945705-CACTGGT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945706_138945711del , CM000665.2:g.138945706_138945711del GRCh38
NC_000003.11:g.138664548_138664553del , CM000665.1:g.138664548_138664553del GRCh37
NC_000003.10:g.140147238_140147243del NCBI36
NG_012454.1:g.6430_6435del
NG_029796.1:g.3473_3478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1012_1017del MANE Select ENSP00000497217.1:p.Thr338_Ser339del
ENST00000330315.3:c.1012_1017del ENSP00000333188.3:p.Thr338_Ser339del
NM_023067.3:c.1012_1017del NP_075555.1:p.Thr338_Ser339del
NM_023067.4:c.1012_1017del MANE Select NP_075555.1:p.Thr338_Ser339del
Search 100 bp 5'
Search 100 bp 3'