Canonical Allele Identifier: CA2647993744
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313888del , CM000663.2:g.152313888del GRCh38
NC_000001.10:g.152286364del , CM000663.1:g.152286364del GRCh37
NC_000001.9:g.150552988del NCBI36
NG_016190.1:g.16317del , LRG_1028:g.16317del

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.999del MANE Select ENSP00000357789.1:p.Arg334AspfsTer?
ENST00000368799.1:c.999del ENSP00000357789.1:p.Arg334AspfsTer?
NM_002016.1:c.999del , LRG_1028t1:c.999del NP_002007.1:p.Arg334AspfsTer?
NR_103778.1:n.430del
XM_011509329.1:c.999del XP_011507631.1:p.Arg334AspfsTer?
NM_002016.2:c.999del MANE Select NP_002007.1:p.Arg334AspfsTer?