Canonical Allele Identifier: CA2479951817
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312243_152312249delinsATCAGAC , CM000663.2:g.152312243_152312249delinsATCAGAC GRCh38
NC_000001.10:g.152284719_152284725delinsATCAGAC , CM000663.1:g.152284719_152284725delinsATCAGAC GRCh37
NC_000001.9:g.150551343_150551349delinsATCAGAC NCBI36
NG_016190.1:g.17955_17961delinsGTCTGAT , LRG_1028:g.17955_17961delinsGTCTGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2637_2643delinsGTCTGAT MANE Select ENSP00000357789.1:p.Arg879=
ENST00000368799.1:c.2637_2643delinsGTCTGAT ENSP00000357789.1:p.Arg879=
NM_002016.1:c.2637_2643delinsGTCTGAT , LRG_1028t1:c.2637_2643delinsGTCTGAT NP_002007.1:p.Arg879=
XM_011509329.1:c.2637_2643delinsGTCTGAT XP_011507631.1:p.Arg879=
NM_002016.2:c.2637_2643delinsGTCTGAT MANE Select NP_002007.1:p.Arg879=