Canonical Allele Identifier: CA2479947479
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304507G= , CM000663.2:g.152304507G= GRCh38
NC_000001.10:g.152276983G= , CM000663.1:g.152276983G= GRCh37
NC_000001.9:g.150543607G= NCBI36
NG_016190.1:g.25697C= , LRG_1028:g.25697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10379C= MANE Select ENSP00000357789.1:p.Ser3460=
ENST00000368799.1:c.10379C= ENSP00000357789.1:p.Ser3460=
NM_002016.1:c.10379C= , LRG_1028t1:c.10379C= NP_002007.1:p.Ser3460=
XM_011509329.1:c.9109-674C= XP_011507631.1:n.9109-674C=
NM_002016.2:c.10379C= MANE Select NP_002007.1:p.Ser3460=