Canonical Allele Identifier: CA1142094645

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304246C= , CM000663.2:g.152304246C=	GRCh38
NC_000001.10:g.152276722C= , CM000663.1:g.152276722C=	GRCh37
NC_000001.9:g.150543346C=	NCBI36
NG_016190.1:g.25958G= , LRG_1028:g.25958G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10640G= MANE Select	ENSP00000357789.1:p.Gly3547=
ENST00000368799.1:c.10640G=	ENSP00000357789.1:p.Gly3547=
NM_002016.1:c.10640G= , LRG_1028t1:c.10640G=	NP_002007.1:p.Gly3547=
XM_011509329.1:c.9109-413G=	XP_011507631.1:n.9109-413G=
NM_002016.2:c.10640G= MANE Select	NP_002007.1:p.Gly3547=