Canonical Allele Identifier: CA1142156918

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152308668T= , CM000663.2:g.152308668T=	GRCh38
NC_000001.10:g.152281144T= , CM000663.1:g.152281144T=	GRCh37
NC_000001.9:g.150547768T=	NCBI36
NG_016190.1:g.21536A= , LRG_1028:g.21536A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6218A= MANE Select	ENSP00000357789.1:p.Lys2073=
ENST00000368799.1:c.6218A=	ENSP00000357789.1:p.Lys2073=
NM_002016.1:c.6218A= , LRG_1028t1:c.6218A=	NP_002007.1:p.Lys2073=
XM_011509329.1:c.6218A=	XP_011507631.1:p.Lys2073=
NM_002016.2:c.6218A= MANE Select	NP_002007.1:p.Lys2073=