Canonical Allele Identifier: CA1143751940

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309018G= , CM000663.2:g.152309018G=	GRCh38
NC_000001.10:g.152281494G= , CM000663.1:g.152281494G=	GRCh37
NC_000001.9:g.150548118G=	NCBI36
NG_016190.1:g.21186C= , LRG_1028:g.21186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5868C= MANE Select	ENSP00000357789.1:p.His1956=
ENST00000368799.1:c.5868C=	ENSP00000357789.1:p.His1956=
NM_002016.1:c.5868C= , LRG_1028t1:c.5868C=	NP_002007.1:p.His1956=
XM_011509329.1:c.5868C=	XP_011507631.1:p.His1956=
NM_002016.2:c.5868C= MANE Select	NP_002007.1:p.His1956=