Canonical Allele Identifier: CA2479947762
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304995_152304996delinsAC , CM000663.2:g.152304995_152304996delinsAC GRCh38
NC_000001.10:g.152277471_152277472delinsAC , CM000663.1:g.152277471_152277472delinsAC GRCh37
NC_000001.9:g.150544095_150544096delinsAC NCBI36
NG_016190.1:g.25208_25209delinsGT , LRG_1028:g.25208_25209delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9890_9891delinsGT MANE Select ENSP00000357789.1:p.Ser3297=
ENST00000368799.1:c.9890_9891delinsGT ENSP00000357789.1:p.Ser3297=
NM_002016.1:c.9890_9891delinsGT , LRG_1028t1:c.9890_9891delinsGT NP_002007.1:p.Ser3297=
XM_011509329.1:c.9108+782_9108+783delinsGT XP_011507631.1:n.9108+782_9108+783delinsGT
NM_002016.2:c.9890_9891delinsGT MANE Select NP_002007.1:p.Ser3297=