Canonical Allele Identifier: CA1142154828
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304742G= , CM000663.2:g.152304742G= GRCh38
NC_000001.10:g.152277218G= , CM000663.1:g.152277218G= GRCh37
NC_000001.9:g.150543842G= NCBI36
NG_016190.1:g.25462C= , LRG_1028:g.25462C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10144C= MANE Select ENSP00000357789.1:p.Arg3382=
ENST00000368799.1:c.10144C= ENSP00000357789.1:p.Arg3382=
NM_002016.1:c.10144C= , LRG_1028t1:c.10144C= NP_002007.1:p.Arg3382=
XM_011509329.1:c.9109-909C= XP_011507631.1:n.9109-909C=
NM_002016.2:c.10144C= MANE Select NP_002007.1:p.Arg3382=