Canonical Allele Identifier: CA2479949285
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307715_152307716delinsGC , CM000663.2:g.152307715_152307716delinsGC GRCh38
NC_000001.10:g.152280191_152280192delinsGC , CM000663.1:g.152280191_152280192delinsGC GRCh37
NC_000001.9:g.150546815_150546816delinsGC NCBI36
NG_016190.1:g.22488_22489delinsGC , LRG_1028:g.22488_22489delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7170_7171delinsGC MANE Select ENSP00000357789.1:p.Gly2390=
ENST00000368799.1:c.7170_7171delinsGC ENSP00000357789.1:p.Gly2390=
NM_002016.1:c.7170_7171delinsGC , LRG_1028t1:c.7170_7171delinsGC NP_002007.1:p.Gly2390=
XM_011509329.1:c.7170_7171delinsGC XP_011507631.1:p.Gly2390=
NM_002016.2:c.7170_7171delinsGC MANE Select NP_002007.1:p.Gly2390=