Canonical Allele Identifier: CA2647993503
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304519del , CM000663.2:g.152304519del GRCh38
NC_000001.10:g.152276995del , CM000663.1:g.152276995del GRCh37
NC_000001.9:g.150543619del NCBI36
NG_016190.1:g.25686del , LRG_1028:g.25686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10368del MANE Select ENSP00000357789.1:p.Arg3456SerfsTer?
ENST00000368799.1:c.10368del ENSP00000357789.1:p.Arg3456SerfsTer?
NM_002016.1:c.10368del , LRG_1028t1:c.10368del NP_002007.1:p.Arg3456SerfsTer?
XM_011509329.1:c.9109-685del XP_011507631.1:n.9109-685del
NM_002016.2:c.10368del MANE Select NP_002007.1:p.Arg3456SerfsTer?