Canonical Allele Identifier: CA1143688361

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313907C= , CM000663.2:g.152313907C=	GRCh38
NC_000001.10:g.152286383C= , CM000663.1:g.152286383C=	GRCh37
NC_000001.9:g.150553007C=	NCBI36
NG_016190.1:g.16297G= , LRG_1028:g.16297G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.979G= MANE Select	ENSP00000357789.1:p.Glu327=
ENST00000368799.1:c.979G=	ENSP00000357789.1:p.Glu327=
NM_002016.1:c.979G= , LRG_1028t1:c.979G=	NP_002007.1:p.Glu327=
NR_103778.1:n.449C=
XM_011509329.1:c.979G=	XP_011507631.1:p.Glu327=
NM_002016.2:c.979G= MANE Select	NP_002007.1:p.Glu327=