Canonical Allele Identifier: CA2479947568
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304672G= , CM000663.2:g.152304672G= GRCh38
NC_000001.10:g.152277148G= , CM000663.1:g.152277148G= GRCh37
NC_000001.9:g.150543772G= NCBI36
NG_016190.1:g.25532C= , LRG_1028:g.25532C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10214C= MANE Select ENSP00000357789.1:p.Thr3405=
ENST00000368799.1:c.10214C= ENSP00000357789.1:p.Thr3405=
NM_002016.1:c.10214C= , LRG_1028t1:c.10214C= NP_002007.1:p.Thr3405=
XM_011509329.1:c.9109-839C= XP_011507631.1:n.9109-839C=
NM_002016.2:c.10214C= MANE Select NP_002007.1:p.Thr3405=