Canonical Allele Identifier: CA2479947540
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304633_152304634delinsGC , CM000663.2:g.152304633_152304634delinsGC GRCh38
NC_000001.10:g.152277109_152277110delinsGC , CM000663.1:g.152277109_152277110delinsGC GRCh37
NC_000001.9:g.150543733_150543734delinsGC NCBI36
NG_016190.1:g.25570_25571delinsGC , LRG_1028:g.25570_25571delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10252_10253delinsGC MANE Select ENSP00000357789.1:p.Ala3418=
ENST00000368799.1:c.10252_10253delinsGC ENSP00000357789.1:p.Ala3418=
NM_002016.1:c.10252_10253delinsGC , LRG_1028t1:c.10252_10253delinsGC NP_002007.1:p.Ala3418=
XM_011509329.1:c.9109-801_9109-800delinsGC XP_011507631.1:n.9109-801_9109-800delinsGC
NM_002016.2:c.10252_10253delinsGC MANE Select NP_002007.1:p.Ala3418=