Canonical Allele Identifier: CA1103353
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs755158954

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304454del , CM000663.2:g.152304454del GRCh38
NC_000001.10:g.152276930del , CM000663.1:g.152276930del GRCh37
NC_000001.9:g.150543554del NCBI36
NG_016190.1:g.25752del , LRG_1028:g.25752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10434del MANE Select ENSP00000357789.1:p.Gln3479SerfsTer?
ENST00000368799.1:c.10434del ENSP00000357789.1:p.Gln3479SerfsTer?
NM_002016.1:c.10434del , LRG_1028t1:c.10434del NP_002007.1:p.Gln3479SerfsTer?
XM_011509329.1:c.9109-619del XP_011507631.1:n.9109-619del
NM_002016.2:c.10434del MANE Select NP_002007.1:p.Gln3479SerfsTer?