Canonical Allele Identifier: CA916310999
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1553213592

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312410_152312411insA , CM000663.2:g.152312410_152312411insA GRCh38
NC_000001.10:g.152284886_152284887insA , CM000663.1:g.152284886_152284887insA GRCh37
NC_000001.9:g.150551510_150551511insA NCBI36
NG_016190.1:g.17793_17794insT , LRG_1028:g.17793_17794insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2475_2476insT MANE Select ENSP00000357789.1:p.Arg826SerfsTer?
ENST00000368799.1:c.2475_2476insT ENSP00000357789.1:p.Arg826SerfsTer?
NM_002016.1:c.2475_2476insT , LRG_1028t1:c.2475_2476insT NP_002007.1:p.Arg826SerfsTer?
XM_011509329.1:c.2475_2476insT XP_011507631.1:p.Arg826SerfsTer?
NM_002016.2:c.2475_2476insT MANE Select NP_002007.1:p.Arg826SerfsTer?