Canonical Allele Identifier: CA1140788899
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312317G= , CM000663.2:g.152312317G= GRCh38
NC_000001.10:g.152284793G= , CM000663.1:g.152284793G= GRCh37
NC_000001.9:g.150551417G= NCBI36
NG_016190.1:g.17887C= , LRG_1028:g.17887C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2569C= MANE Select ENSP00000357789.1:p.His857=
ENST00000368799.1:c.2569C= ENSP00000357789.1:p.His857=
NM_002016.1:c.2569C= , LRG_1028t1:c.2569C= NP_002007.1:p.His857=
XM_011509329.1:c.2569C= XP_011507631.1:p.His857=
NM_002016.2:c.2569C= MANE Select NP_002007.1:p.His857=