Canonical Allele Identifier: CA1007766385
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307692del , CM000663.2:g.152307692del GRCh38
NC_000001.10:g.152280168del , CM000663.1:g.152280168del GRCh37
NC_000001.9:g.150546792del NCBI36
NG_016190.1:g.22512del , LRG_1028:g.22512del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7194del MANE Select ENSP00000357789.1:p.Glu2398AspfsTer21
ENST00000368799.1:c.7194del ENSP00000357789.1:p.Glu2398AspfsTer21
NM_002016.1:c.7194del , LRG_1028t1:c.7194del NP_002007.1:p.Glu2398AspfsTer21
XM_011509329.1:c.7194del XP_011507631.1:p.Glu2398AspfsTer21
NM_002016.2:c.7194del MANE Select NP_002007.1:p.Glu2398AspfsTer21