Canonical Allele Identifier: CA2479949334

Gene: FLG

Linked Data

• dbSNP Id: rs1652084392
• gnomAD v4: 1-152307815-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307819_152307820del , CM000663.2:g.152307819_152307820del	GRCh38
NC_000001.10:g.152280295_152280296del , CM000663.1:g.152280295_152280296del	GRCh37
NC_000001.9:g.150546919_150546920del	NCBI36
NG_016190.1:g.22387_22388del , LRG_1028:g.22387_22388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.7069_7070del MANE Select	ENSP00000357789.1:p.Asp2357GlnfsTer9
ENST00000368799.1:c.7069_7070del	ENSP00000357789.1:p.Asp2357GlnfsTer9
NM_002016.1:c.7069_7070del , LRG_1028t1:c.7069_7070del	NP_002007.1:p.Asp2357GlnfsTer9
XM_011509329.1:c.7069_7070del	XP_011507631.1:p.Asp2357GlnfsTer9
NM_002016.2:c.7069_7070del MANE Select	NP_002007.1:p.Asp2357GlnfsTer9