Canonical Allele Identifier: CA2479947805
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305067_152305071delinsTTGTC , CM000663.2:g.152305067_152305071delinsTTGTC GRCh38
NC_000001.10:g.152277543_152277547delinsTTGTC , CM000663.1:g.152277543_152277547delinsTTGTC GRCh37
NC_000001.9:g.150544167_150544171delinsTTGTC NCBI36
NG_016190.1:g.25133_25137delinsGACAA , LRG_1028:g.25133_25137delinsGACAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9815_9819delinsGACAA MANE Select ENSP00000357789.1:p.Arg3272=
ENST00000368799.1:c.9815_9819delinsGACAA ENSP00000357789.1:p.Arg3272=
NM_002016.1:c.9815_9819delinsGACAA , LRG_1028t1:c.9815_9819delinsGACAA NP_002007.1:p.Arg3272=
XM_011509329.1:c.9108+707_9108+711delinsGACAA XP_011507631.1:n.9108+707_9108+711delinsGACAA
NM_002016.2:c.9815_9819delinsGACAA MANE Select NP_002007.1:p.Arg3272=
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