Canonical Allele Identifier: CA2479947796
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305050G= , CM000663.2:g.152305050G= GRCh38
NC_000001.10:g.152277526G= , CM000663.1:g.152277526G= GRCh37
NC_000001.9:g.150544150G= NCBI36
NG_016190.1:g.25154C= , LRG_1028:g.25154C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9836C= MANE Select ENSP00000357789.1:p.Ala3279=
ENST00000368799.1:c.9836C= ENSP00000357789.1:p.Ala3279=
NM_002016.1:c.9836C= , LRG_1028t1:c.9836C= NP_002007.1:p.Ala3279=
XM_011509329.1:c.9108+728C= XP_011507631.1:n.9108+728C=
NM_002016.2:c.9836C= MANE Select NP_002007.1:p.Ala3279=