Canonical Allele Identifier: CA2647993646

Gene: FLG

Linked Data

• gnomAD v4: 1-152309100-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309101del , CM000663.2:g.152309101del	GRCh38
NC_000001.10:g.152281577del , CM000663.1:g.152281577del	GRCh37
NC_000001.9:g.150548201del	NCBI36
NG_016190.1:g.21103del , LRG_1028:g.21103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5785del MANE Select	ENSP00000357789.1:p.Glu1929LysfsTer?
ENST00000368799.1:c.5785del	ENSP00000357789.1:p.Glu1929LysfsTer?
NM_002016.1:c.5785del , LRG_1028t1:c.5785del	NP_002007.1:p.Glu1929LysfsTer?
XM_011509329.1:c.5785del	XP_011507631.1:p.Glu1929LysfsTer?
NM_002016.2:c.5785del MANE Select	NP_002007.1:p.Glu1929LysfsTer?