Canonical Allele Identifier: CA2746124213
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309145_152309146insC , CM000663.2:g.152309145_152309146insC GRCh38
NC_000001.10:g.152281621_152281622insC , CM000663.1:g.152281621_152281622insC GRCh37
NC_000001.9:g.150548245_150548246insC NCBI36
NG_016190.1:g.21058_21059insG , LRG_1028:g.21058_21059insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5740_5741insG MANE Select ENSP00000357789.1:p.Gln1914ArgfsTer6
ENST00000368799.1:c.5740_5741insG ENSP00000357789.1:p.Gln1914ArgfsTer6
NM_002016.1:c.5740_5741insG , LRG_1028t1:c.5740_5741insG NP_002007.1:p.Gln1914ArgfsTer6
XM_011509329.1:c.5740_5741insG XP_011507631.1:p.Gln1914ArgfsTer6
NM_002016.2:c.5740_5741insG MANE Select NP_002007.1:p.Gln1914ArgfsTer6