Canonical Allele Identifier: CA2574058027
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309194_152309197dup , CM000663.2:g.152309194_152309197dup GRCh38
NC_000001.10:g.152281670_152281673dup , CM000663.1:g.152281670_152281673dup GRCh37
NC_000001.9:g.150548294_150548297dup NCBI36
NG_016190.1:g.21008_21011dup , LRG_1028:g.21008_21011dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5690_5693dup MANE Select ENSP00000357789.1:p.Gln1899LeufsTer22
ENST00000368799.1:c.5690_5693dup ENSP00000357789.1:p.Gln1899LeufsTer22
NM_002016.1:c.5690_5693dup , LRG_1028t1:c.5690_5693dup NP_002007.1:p.Gln1899LeufsTer22
XM_011509329.1:c.5690_5693dup XP_011507631.1:p.Gln1899LeufsTer22
NM_002016.2:c.5690_5693dup MANE Select NP_002007.1:p.Gln1899LeufsTer22