Canonical Allele Identifier: CA2479947619
Gene: FLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304752_152304753delinsTC , CM000663.2:g.152304752_152304753delinsTC GRCh38
NC_000001.10:g.152277228_152277229delinsTC , CM000663.1:g.152277228_152277229delinsTC GRCh37
NC_000001.9:g.150543852_150543853delinsTC NCBI36
NG_016190.1:g.25451_25452delinsGA , LRG_1028:g.25451_25452delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10133_10134delinsGA MANE Select ENSP00000357789.1:p.Gly3378=
ENST00000368799.1:c.10133_10134delinsGA ENSP00000357789.1:p.Gly3378=
NM_002016.1:c.10133_10134delinsGA , LRG_1028t1:c.10133_10134delinsGA NP_002007.1:p.Gly3378=
XM_011509329.1:c.9109-920_9109-919delinsGA XP_011507631.1:n.9109-920_9109-919delinsGA
NM_002016.2:c.10133_10134delinsGA MANE Select NP_002007.1:p.Gly3378=
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Search 100 bp 3'