Canonical Allele Identifier: CA2479947532
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304616_152304617delinsGC , CM000663.2:g.152304616_152304617delinsGC GRCh38
NC_000001.10:g.152277092_152277093delinsGC , CM000663.1:g.152277092_152277093delinsGC GRCh37
NC_000001.9:g.150543716_150543717delinsGC NCBI36
NG_016190.1:g.25587_25588delinsGC , LRG_1028:g.25587_25588delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10269_10270delinsGC MANE Select ENSP00000357789.1:p.Arg3423=
ENST00000368799.1:c.10269_10270delinsGC ENSP00000357789.1:p.Arg3423=
NM_002016.1:c.10269_10270delinsGC , LRG_1028t1:c.10269_10270delinsGC NP_002007.1:p.Arg3423=
XM_011509329.1:c.9109-784_9109-783delinsGC XP_011507631.1:n.9109-784_9109-783delinsGC
NM_002016.2:c.10269_10270delinsGC MANE Select NP_002007.1:p.Arg3423=