Canonical Allele Identifier: CA1146266398

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152308616G= , CM000663.2:g.152308616G=	GRCh38
NC_000001.10:g.152281092G= , CM000663.1:g.152281092G=	GRCh37
NC_000001.9:g.150547716G=	NCBI36
NG_016190.1:g.21588C= , LRG_1028:g.21588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6270C= MANE Select	ENSP00000357789.1:p.Phe2090=
ENST00000368799.1:c.6270C=	ENSP00000357789.1:p.Phe2090=
NM_002016.1:c.6270C= , LRG_1028t1:c.6270C=	NP_002007.1:p.Phe2090=
XM_011509329.1:c.6270C=	XP_011507631.1:p.Phe2090=
NM_002016.2:c.6270C= MANE Select	NP_002007.1:p.Phe2090=