Canonical Allele Identifier: CA2479950077
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309084C= , CM000663.2:g.152309084C= GRCh38
NC_000001.10:g.152281560C= , CM000663.1:g.152281560C= GRCh37
NC_000001.9:g.150548184C= NCBI36
NG_016190.1:g.21120G= , LRG_1028:g.21120G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5802G= MANE Select ENSP00000357789.1:p.Trp1934=
ENST00000368799.1:c.5802G= ENSP00000357789.1:p.Trp1934=
NM_002016.1:c.5802G= , LRG_1028t1:c.5802G= NP_002007.1:p.Trp1934=
XM_011509329.1:c.5802G= XP_011507631.1:p.Trp1934=
NM_002016.2:c.5802G= MANE Select NP_002007.1:p.Trp1934=