Canonical Allele Identifier: CA2479951430
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311555_152311556delinsAC , CM000663.2:g.152311555_152311556delinsAC GRCh38
NC_000001.10:g.152284031_152284032delinsAC , CM000663.1:g.152284031_152284032delinsAC GRCh37
NC_000001.9:g.150550655_150550656delinsAC NCBI36
NG_016190.1:g.18648_18649delinsGT , LRG_1028:g.18648_18649delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3330_3331delinsGT MANE Select ENSP00000357789.1:p.Arg1110=
ENST00000368799.1:c.3330_3331delinsGT ENSP00000357789.1:p.Arg1110=
NM_002016.1:c.3330_3331delinsGT , LRG_1028t1:c.3330_3331delinsGT NP_002007.1:p.Arg1110=
XM_011509329.1:c.3330_3331delinsGT XP_011507631.1:p.Arg1110=
NM_002016.2:c.3330_3331delinsGT MANE Select NP_002007.1:p.Arg1110=