Canonical Allele Identifier: CA2479947799
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305057G= , CM000663.2:g.152305057G= GRCh38
NC_000001.10:g.152277533G= , CM000663.1:g.152277533G= GRCh37
NC_000001.9:g.150544157G= NCBI36
NG_016190.1:g.25147C= , LRG_1028:g.25147C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9829C= MANE Select ENSP00000357789.1:p.Arg3277=
ENST00000368799.1:c.9829C= ENSP00000357789.1:p.Arg3277=
NM_002016.1:c.9829C= , LRG_1028t1:c.9829C= NP_002007.1:p.Arg3277=
XM_011509329.1:c.9108+721C= XP_011507631.1:n.9108+721C=
NM_002016.2:c.9829C= MANE Select NP_002007.1:p.Arg3277=