Canonical Allele Identifier: CA2479951934

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312480_152312484delinsCTGTT , CM000663.2:g.152312480_152312484delinsCTGTT	GRCh38
NC_000001.10:g.152284956_152284960delinsCTGTT , CM000663.1:g.152284956_152284960delinsCTGTT	GRCh37
NC_000001.9:g.150551580_150551584delinsCTGTT	NCBI36
NG_016190.1:g.17720_17724delinsAACAG , LRG_1028:g.17720_17724delinsAACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2402_2406delinsAACAG MANE Select	ENSP00000357789.1:p.Lys801=
ENST00000368799.1:c.2402_2406delinsAACAG	ENSP00000357789.1:p.Lys801=
NM_002016.1:c.2402_2406delinsAACAG , LRG_1028t1:c.2402_2406delinsAACAG	NP_002007.1:p.Lys801=
XM_011509329.1:c.2402_2406delinsAACAG	XP_011507631.1:p.Lys801=
NM_002016.2:c.2402_2406delinsAACAG MANE Select	NP_002007.1:p.Lys801=