Canonical Allele Identifier: CA2479950141

Gene: FLG

Linked Data

• dbSNP Id: rs1652210017

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309192del , CM000663.2:g.152309192del	GRCh38
NC_000001.10:g.152281668del , CM000663.1:g.152281668del	GRCh37
NC_000001.9:g.150548292del	NCBI36
NG_016190.1:g.21012del , LRG_1028:g.21012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5694del MANE Select	ENSP00000357789.1:p.Gln1899ArgfsTer?
ENST00000368799.1:c.5694del	ENSP00000357789.1:p.Gln1899ArgfsTer?
NM_002016.1:c.5694del , LRG_1028t1:c.5694del	NP_002007.1:p.Gln1899ArgfsTer?
XM_011509329.1:c.5694del	XP_011507631.1:p.Gln1899ArgfsTer?
NM_002016.2:c.5694del MANE Select	NP_002007.1:p.Gln1899ArgfsTer?