Canonical Allele Identifier: CA2479949393

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307930T= , CM000663.2:g.152307930T=	GRCh38
NC_000001.10:g.152280406T= , CM000663.1:g.152280406T=	GRCh37
NC_000001.9:g.150547030T=	NCBI36
NG_016190.1:g.22274A= , LRG_1028:g.22274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6956A= MANE Select	ENSP00000357789.1:p.His2319=
ENST00000368799.1:c.6956A=	ENSP00000357789.1:p.His2319=
NM_002016.1:c.6956A= , LRG_1028t1:c.6956A=	NP_002007.1:p.His2319=
XM_011509329.1:c.6956A=	XP_011507631.1:p.His2319=
NM_002016.2:c.6956A= MANE Select	NP_002007.1:p.His2319=