Canonical Allele Identifier: CA1146938782

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313910A= , CM000663.2:g.152313910A=	GRCh38
NC_000001.10:g.152286386A= , CM000663.1:g.152286386A=	GRCh37
NC_000001.9:g.150553010A=	NCBI36
NG_016190.1:g.16294T= , LRG_1028:g.16294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.976T= MANE Select	ENSP00000357789.1:p.Trp326=
ENST00000368799.1:c.976T=	ENSP00000357789.1:p.Trp326=
NM_002016.1:c.976T= , LRG_1028t1:c.976T=	NP_002007.1:p.Trp326=
NR_103778.1:n.452A=
XM_011509329.1:c.976T=	XP_011507631.1:p.Trp326=
NM_002016.2:c.976T= MANE Select	NP_002007.1:p.Trp326=