Canonical Allele Identifier: CA2479947690
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304867_152304868delinsGC , CM000663.2:g.152304867_152304868delinsGC GRCh38
NC_000001.10:g.152277343_152277344delinsGC , CM000663.1:g.152277343_152277344delinsGC GRCh37
NC_000001.9:g.150543967_150543968delinsGC NCBI36
NG_016190.1:g.25336_25337delinsGC , LRG_1028:g.25336_25337delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10018_10019delinsGC MANE Select ENSP00000357789.1:p.Ala3340=
ENST00000368799.1:c.10018_10019delinsGC ENSP00000357789.1:p.Ala3340=
NM_002016.1:c.10018_10019delinsGC , LRG_1028t1:c.10018_10019delinsGC NP_002007.1:p.Ala3340=
XM_011509329.1:c.9108+910_9108+911delinsGC XP_011507631.1:n.9108+910_9108+911delinsGC
NM_002016.2:c.10018_10019delinsGC MANE Select NP_002007.1:p.Ala3340=
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