Canonical Allele Identifier: CA2479947374
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304301_152304302delinsGC , CM000663.2:g.152304301_152304302delinsGC GRCh38
NC_000001.10:g.152276777_152276778delinsGC , CM000663.1:g.152276777_152276778delinsGC GRCh37
NC_000001.9:g.150543401_150543402delinsGC NCBI36
NG_016190.1:g.25902_25903delinsGC , LRG_1028:g.25902_25903delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10584_10585delinsGC MANE Select ENSP00000357789.1:p.Gly3528=
ENST00000368799.1:c.10584_10585delinsGC ENSP00000357789.1:p.Gly3528=
NM_002016.1:c.10584_10585delinsGC , LRG_1028t1:c.10584_10585delinsGC NP_002007.1:p.Gly3528=
XM_011509329.1:c.9109-469_9109-468delinsGC XP_011507631.1:n.9109-469_9109-468delinsGC
NM_002016.2:c.10584_10585delinsGC MANE Select NP_002007.1:p.Gly3528=
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