Canonical Allele Identifier: CA1149154457

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304237T= , CM000663.2:g.152304237T=	GRCh38
NC_000001.10:g.152276713T= , CM000663.1:g.152276713T=	GRCh37
NC_000001.9:g.150543337T=	NCBI36
NG_016190.1:g.25967A= , LRG_1028:g.25967A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10649A= MANE Select	ENSP00000357789.1:p.Glu3550=
ENST00000368799.1:c.10649A=	ENSP00000357789.1:p.Glu3550=
NM_002016.1:c.10649A= , LRG_1028t1:c.10649A=	NP_002007.1:p.Glu3550=
XM_011509329.1:c.9109-404A=	XP_011507631.1:n.9109-404A=
NM_002016.2:c.10649A= MANE Select	NP_002007.1:p.Glu3550=