Canonical Allele Identifier: CA2479947452
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304451_152304452delinsGC , CM000663.2:g.152304451_152304452delinsGC GRCh38
NC_000001.10:g.152276927_152276928delinsGC , CM000663.1:g.152276927_152276928delinsGC GRCh37
NC_000001.9:g.150543551_150543552delinsGC NCBI36
NG_016190.1:g.25752_25753delinsGC , LRG_1028:g.25752_25753delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10434_10435delinsGC MANE Select ENSP00000357789.1:p.Gly3478=
ENST00000368799.1:c.10434_10435delinsGC ENSP00000357789.1:p.Gly3478=
NM_002016.1:c.10434_10435delinsGC , LRG_1028t1:c.10434_10435delinsGC NP_002007.1:p.Gly3478=
XM_011509329.1:c.9109-619_9109-618delinsGC XP_011507631.1:n.9109-619_9109-618delinsGC
NM_002016.2:c.10434_10435delinsGC MANE Select NP_002007.1:p.Gly3478=