Canonical Allele Identifier: CA2479947794
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305045T= , CM000663.2:g.152305045T= GRCh38
NC_000001.10:g.152277521T= , CM000663.1:g.152277521T= GRCh37
NC_000001.9:g.150544145T= NCBI36
NG_016190.1:g.25159A= , LRG_1028:g.25159A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9841A= MANE Select ENSP00000357789.1:p.Thr3281=
ENST00000368799.1:c.9841A= ENSP00000357789.1:p.Thr3281=
NM_002016.1:c.9841A= , LRG_1028t1:c.9841A= NP_002007.1:p.Thr3281=
XM_011509329.1:c.9108+733A= XP_011507631.1:n.9108+733A=
NM_002016.2:c.9841A= MANE Select NP_002007.1:p.Thr3281=