Canonical Allele Identifier: CA1007766356
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652072683

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307666_152307667insG , CM000663.2:g.152307666_152307667insG GRCh38
NC_000001.10:g.152280142_152280143insG , CM000663.1:g.152280142_152280143insG GRCh37
NC_000001.9:g.150546766_150546767insG NCBI36
NG_016190.1:g.22537_22538insC , LRG_1028:g.22537_22538insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7219_7220insC MANE Select ENSP00000357789.1:p.Arg2407ThrfsTer16
ENST00000368799.1:c.7219_7220insC ENSP00000357789.1:p.Arg2407ThrfsTer16
NM_002016.1:c.7219_7220insC , LRG_1028t1:c.7219_7220insC NP_002007.1:p.Arg2407ThrfsTer16
XM_011509329.1:c.7219_7220insC XP_011507631.1:p.Arg2407ThrfsTer16
NM_002016.2:c.7219_7220insC MANE Select NP_002007.1:p.Arg2407ThrfsTer16