Canonical Allele Identifier: CA2479951941
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312494_152312503delinsTCACCTGGTA , CM000663.2:g.152312494_152312503delinsTCACCTGGTA GRCh38
NC_000001.10:g.152284970_152284979delinsTCACCTGGTA , CM000663.1:g.152284970_152284979delinsTCACCTGGTA GRCh37
NC_000001.9:g.150551594_150551603delinsTCACCTGGTA NCBI36
NG_016190.1:g.17701_17710delinsTACCAGGTGA , LRG_1028:g.17701_17710delinsTACCAGGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2383_2392delinsTACCAGGTGA MANE Select ENSP00000357789.1:p.Tyr795=
ENST00000368799.1:c.2383_2392delinsTACCAGGTGA ENSP00000357789.1:p.Tyr795=
NM_002016.1:c.2383_2392delinsTACCAGGTGA , LRG_1028t1:c.2383_2392delinsTACCAGGTGA NP_002007.1:p.Tyr795=
XM_011509329.1:c.2383_2392delinsTACCAGGTGA XP_011507631.1:p.Tyr795=
NM_002016.2:c.2383_2392delinsTACCAGGTGA MANE Select NP_002007.1:p.Tyr795=