Canonical Allele Identifier: CA2479951011

Gene: FLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310688_152310690delinsCCT , CM000663.2:g.152310688_152310690delinsCCT	GRCh38
NC_000001.10:g.152283164_152283166delinsCCT , CM000663.1:g.152283164_152283166delinsCCT	GRCh37
NC_000001.9:g.150549788_150549790delinsCCT	NCBI36
NG_016190.1:g.19514_19516delinsAGG , LRG_1028:g.19514_19516delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.4196_4198delinsAGG MANE Select	ENSP00000357789.1:p.Glu1399=
ENST00000368799.1:c.4196_4198delinsAGG	ENSP00000357789.1:p.Glu1399=
NM_002016.1:c.4196_4198delinsAGG , LRG_1028t1:c.4196_4198delinsAGG	NP_002007.1:p.Glu1399=
XM_011509329.1:c.4196_4198delinsAGG	XP_011507631.1:p.Glu1399=
NM_002016.2:c.4196_4198delinsAGG MANE Select	NP_002007.1:p.Glu1399=