Canonical Allele Identifier: CA2647993514
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304674_152304675insGCAGA , CM000663.2:g.152304674_152304675insGCAGA GRCh38
NC_000001.10:g.152277150_152277151insGCAGA , CM000663.1:g.152277150_152277151insGCAGA GRCh37
NC_000001.9:g.150543774_150543775insGCAGA NCBI36
NG_016190.1:g.25529_25530insTCTGC , LRG_1028:g.25529_25530insTCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10211_10212insTCTGC MANE Select ENSP00000357789.1:p.Arg3404SerfsTer?
ENST00000368799.1:c.10211_10212insTCTGC ENSP00000357789.1:p.Arg3404SerfsTer?
NM_002016.1:c.10211_10212insTCTGC , LRG_1028t1:c.10211_10212insTCTGC NP_002007.1:p.Arg3404SerfsTer?
XM_011509329.1:c.9109-842_9109-841insTCTGC XP_011507631.1:n.9109-842_9109-841insTCTGC
NM_002016.2:c.10211_10212insTCTGC MANE Select NP_002007.1:p.Arg3404SerfsTer?