Canonical Allele Identifier: CA1146049868
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304762C= , CM000663.2:g.152304762C= GRCh38
NC_000001.10:g.152277238C= , CM000663.1:g.152277238C= GRCh37
NC_000001.9:g.150543862C= NCBI36
NG_016190.1:g.25442G= , LRG_1028:g.25442G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10124G= MANE Select ENSP00000357789.1:p.Arg3375=
ENST00000368799.1:c.10124G= ENSP00000357789.1:p.Arg3375=
NM_002016.1:c.10124G= , LRG_1028t1:c.10124G= NP_002007.1:p.Arg3375=
XM_011509329.1:c.9109-929G= XP_011507631.1:n.9109-929G=
NM_002016.2:c.10124G= MANE Select NP_002007.1:p.Arg3375=