Canonical Allele Identifier: CA1140094308
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304920T= , CM000663.2:g.152304920T= GRCh38
NC_000001.10:g.152277396T= , CM000663.1:g.152277396T= GRCh37
NC_000001.9:g.150544020T= NCBI36
NG_016190.1:g.25284A= , LRG_1028:g.25284A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9966A= MANE Select ENSP00000357789.1:p.Gln3322=
ENST00000368799.1:c.9966A= ENSP00000357789.1:p.Gln3322=
NM_002016.1:c.9966A= , LRG_1028t1:c.9966A= NP_002007.1:p.Gln3322=
XM_011509329.1:c.9108+858A= XP_011507631.1:n.9108+858A=
NM_002016.2:c.9966A= MANE Select NP_002007.1:p.Gln3322=