Canonical Allele Identifier: CA2479950044
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309030A= , CM000663.2:g.152309030A= GRCh38
NC_000001.10:g.152281506A= , CM000663.1:g.152281506A= GRCh37
NC_000001.9:g.150548130A= NCBI36
NG_016190.1:g.21174T= , LRG_1028:g.21174T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5856T= MANE Select ENSP00000357789.1:p.Asp1952=
ENST00000368799.1:c.5856T= ENSP00000357789.1:p.Asp1952=
NM_002016.1:c.5856T= , LRG_1028t1:c.5856T= NP_002007.1:p.Asp1952=
XM_011509329.1:c.5856T= XP_011507631.1:p.Asp1952=
NM_002016.2:c.5856T= MANE Select NP_002007.1:p.Asp1952=