Canonical Allele Identifier: CA2479947386
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304318_152304322delinsTGGCC , CM000663.2:g.152304318_152304322delinsTGGCC GRCh38
NC_000001.10:g.152276794_152276798delinsTGGCC , CM000663.1:g.152276794_152276798delinsTGGCC GRCh37
NC_000001.9:g.150543418_150543422delinsTGGCC NCBI36
NG_016190.1:g.25882_25886delinsGGCCA , LRG_1028:g.25882_25886delinsGGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10564_10568delinsGGCCA MANE Select ENSP00000357789.1:p.Gly3522=
ENST00000368799.1:c.10564_10568delinsGGCCA ENSP00000357789.1:p.Gly3522=
NM_002016.1:c.10564_10568delinsGGCCA , LRG_1028t1:c.10564_10568delinsGGCCA NP_002007.1:p.Gly3522=
XM_011509329.1:c.9109-489_9109-485delinsGGCCA XP_011507631.1:n.9109-489_9109-485delinsGGCCA
NM_002016.2:c.10564_10568delinsGGCCA MANE Select NP_002007.1:p.Gly3522=
Search 100 bp 5'
Search 100 bp 3'