Canonical Allele Identifier: CA2479952775
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152314012G= , CM000663.2:g.152314012G= GRCh38
NC_000001.10:g.152286488G= , CM000663.1:g.152286488G= GRCh37
NC_000001.9:g.150553112G= NCBI36
NG_016190.1:g.16192C= , LRG_1028:g.16192C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.874C= MANE Select ENSP00000357789.1:p.Arg292=
ENST00000368799.1:c.874C= ENSP00000357789.1:p.Arg292=
NM_002016.1:c.874C= , LRG_1028t1:c.874C= NP_002007.1:p.Arg292=
NR_103778.1:n.554G=
XM_011509329.1:c.874C= XP_011507631.1:p.Arg292=
NM_002016.2:c.874C= MANE Select NP_002007.1:p.Arg292=