Canonical Allele Identifier: CA2479947700
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304883_152304884delinsAC , CM000663.2:g.152304883_152304884delinsAC GRCh38
NC_000001.10:g.152277359_152277360delinsAC , CM000663.1:g.152277359_152277360delinsAC GRCh37
NC_000001.9:g.150543983_150543984delinsAC NCBI36
NG_016190.1:g.25320_25321delinsGT , LRG_1028:g.25320_25321delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10002_10003delinsGT MANE Select ENSP00000357789.1:p.Gly3334=
ENST00000368799.1:c.10002_10003delinsGT ENSP00000357789.1:p.Gly3334=
NM_002016.1:c.10002_10003delinsGT , LRG_1028t1:c.10002_10003delinsGT NP_002007.1:p.Gly3334=
XM_011509329.1:c.9108+894_9108+895delinsGT XP_011507631.1:n.9108+894_9108+895delinsGT
NM_002016.2:c.10002_10003delinsGT MANE Select NP_002007.1:p.Gly3334=
Search 100 bp 5'
Search 100 bp 3'