Canonical Allele Identifier: CA2479951348

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311394G= , CM000663.2:g.152311394G=	GRCh38
NC_000001.10:g.152283870G= , CM000663.1:g.152283870G=	GRCh37
NC_000001.9:g.150550494G=	NCBI36
NG_016190.1:g.18810C= , LRG_1028:g.18810C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3492C= MANE Select	ENSP00000357789.1:p.Thr1164=
ENST00000368799.1:c.3492C=	ENSP00000357789.1:p.Thr1164=
NM_002016.1:c.3492C= , LRG_1028t1:c.3492C=	NP_002007.1:p.Thr1164=
XM_011509329.1:c.3492C=	XP_011507631.1:p.Thr1164=
NM_002016.2:c.3492C= MANE Select	NP_002007.1:p.Thr1164=