Canonical Allele Identifier: CA2479947387

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304319G= , CM000663.2:g.152304319G=	GRCh38
NC_000001.10:g.152276795G= , CM000663.1:g.152276795G=	GRCh37
NC_000001.9:g.150543419G=	NCBI36
NG_016190.1:g.25885C= , LRG_1028:g.25885C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10567C= MANE Select	ENSP00000357789.1:p.Gln3523=
ENST00000368799.1:c.10567C=	ENSP00000357789.1:p.Gln3523=
NM_002016.1:c.10567C= , LRG_1028t1:c.10567C=	NP_002007.1:p.Gln3523=
XM_011509329.1:c.9109-486C=	XP_011507631.1:n.9109-486C=
NM_002016.2:c.10567C= MANE Select	NP_002007.1:p.Gln3523=