Canonical Allele Identifier: CA1144114380
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312327C= , CM000663.2:g.152312327C= GRCh38
NC_000001.10:g.152284803C= , CM000663.1:g.152284803C= GRCh37
NC_000001.9:g.150551427C= NCBI36
NG_016190.1:g.17877G= , LRG_1028:g.17877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2559G= MANE Select ENSP00000357789.1:p.Gln853=
ENST00000368799.1:c.2559G= ENSP00000357789.1:p.Gln853=
NM_002016.1:c.2559G= , LRG_1028t1:c.2559G= NP_002007.1:p.Gln853=
XM_011509329.1:c.2559G= XP_011507631.1:p.Gln853=
NM_002016.2:c.2559G= MANE Select NP_002007.1:p.Gln853=