Canonical Allele Identifier: CA1146514491

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309187A= , CM000663.2:g.152309187A=	GRCh38
NC_000001.10:g.152281663A= , CM000663.1:g.152281663A=	GRCh37
NC_000001.9:g.150548287A=	NCBI36
NG_016190.1:g.21017T= , LRG_1028:g.21017T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5699T= MANE Select	ENSP00000357789.1:p.Val1900=
ENST00000368799.1:c.5699T=	ENSP00000357789.1:p.Val1900=
NM_002016.1:c.5699T= , LRG_1028t1:c.5699T=	NP_002007.1:p.Val1900=
XM_011509329.1:c.5699T=	XP_011507631.1:p.Val1900=
NM_002016.2:c.5699T= MANE Select	NP_002007.1:p.Val1900=