Canonical Allele Identifier: CA1141628153
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312456T= , CM000663.2:g.152312456T= GRCh38
NC_000001.10:g.152284932T= , CM000663.1:g.152284932T= GRCh37
NC_000001.9:g.150551556T= NCBI36
NG_016190.1:g.17748A= , LRG_1028:g.17748A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2430A= MANE Select ENSP00000357789.1:p.Thr810=
ENST00000368799.1:c.2430A= ENSP00000357789.1:p.Thr810=
NM_002016.1:c.2430A= , LRG_1028t1:c.2430A= NP_002007.1:p.Thr810=
XM_011509329.1:c.2430A= XP_011507631.1:p.Thr810=
NM_002016.2:c.2430A= MANE Select NP_002007.1:p.Thr810=