Canonical Allele Identifier: CA1148876037

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307988T= , CM000663.2:g.152307988T=	GRCh38
NC_000001.10:g.152280464T= , CM000663.1:g.152280464T=	GRCh37
NC_000001.9:g.150547088T=	NCBI36
NG_016190.1:g.22216A= , LRG_1028:g.22216A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6898A= MANE Select	ENSP00000357789.1:p.Arg2300=
ENST00000368799.1:c.6898A=	ENSP00000357789.1:p.Arg2300=
NM_002016.1:c.6898A= , LRG_1028t1:c.6898A=	NP_002007.1:p.Arg2300=
XM_011509329.1:c.6898A=	XP_011507631.1:p.Arg2300=
NM_002016.2:c.6898A= MANE Select	NP_002007.1:p.Arg2300=