Canonical Allele Identifier: CA916311162
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1557871290

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304678del , CM000663.2:g.152304678del GRCh38
NC_000001.10:g.152277154del , CM000663.1:g.152277154del GRCh37
NC_000001.9:g.150543778del NCBI36
NG_016190.1:g.25527del , LRG_1028:g.25527del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10209del MANE Select ENSP00000357789.1:p.Arg3404GlyfsTer?
ENST00000368799.1:c.10209del ENSP00000357789.1:p.Arg3404GlyfsTer?
NM_002016.1:c.10209del , LRG_1028t1:c.10209del NP_002007.1:p.Arg3404GlyfsTer?
XM_011509329.1:c.9109-844del XP_011507631.1:n.9109-844del
NM_002016.2:c.10209del MANE Select NP_002007.1:p.Arg3404GlyfsTer?