Canonical Allele Identifier: CA2479949252
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307651C= , CM000663.2:g.152307651C= GRCh38
NC_000001.10:g.152280127C= , CM000663.1:g.152280127C= GRCh37
NC_000001.9:g.150546751C= NCBI36
NG_016190.1:g.22553G= , LRG_1028:g.22553G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7235G= MANE Select ENSP00000357789.1:p.Gly2412=
ENST00000368799.1:c.7235G= ENSP00000357789.1:p.Gly2412=
NM_002016.1:c.7235G= , LRG_1028t1:c.7235G= NP_002007.1:p.Gly2412=
XM_011509329.1:c.7235G= XP_011507631.1:p.Gly2412=
NM_002016.2:c.7235G= MANE Select NP_002007.1:p.Gly2412=