Canonical Allele Identifier: CA526662128
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1332278726

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304757del , CM000663.2:g.152304757del GRCh38
NC_000001.10:g.152277233del , CM000663.1:g.152277233del GRCh37
NC_000001.9:g.150543857del NCBI36
NG_016190.1:g.25451del , LRG_1028:g.25451del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10133del MANE Select ENSP00000357789.1:p.Gly3378GlufsTer13
ENST00000368799.1:c.10133del ENSP00000357789.1:p.Gly3378GlufsTer13
NM_002016.1:c.10133del , LRG_1028t1:c.10133del NP_002007.1:p.Gly3378GlufsTer13
XM_011509329.1:c.9109-920del XP_011507631.1:n.9109-920del
NM_002016.2:c.10133del MANE Select NP_002007.1:p.Gly3378GlufsTer13