Canonical Allele Identifier: CA2479947752
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304977_152304978delinsTC , CM000663.2:g.152304977_152304978delinsTC GRCh38
NC_000001.10:g.152277453_152277454delinsTC , CM000663.1:g.152277453_152277454delinsTC GRCh37
NC_000001.9:g.150544077_150544078delinsTC NCBI36
NG_016190.1:g.25226_25227delinsGA , LRG_1028:g.25226_25227delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9908_9909delinsGA MANE Select ENSP00000357789.1:p.Gly3303=
ENST00000368799.1:c.9908_9909delinsGA ENSP00000357789.1:p.Gly3303=
NM_002016.1:c.9908_9909delinsGA , LRG_1028t1:c.9908_9909delinsGA NP_002007.1:p.Gly3303=
XM_011509329.1:c.9108+800_9108+801delinsGA XP_011507631.1:n.9108+800_9108+801delinsGA
NM_002016.2:c.9908_9909delinsGA MANE Select NP_002007.1:p.Gly3303=
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Search 100 bp 3'