Canonical Allele Identifier: CA1007766366

Gene: FLG

Linked Data

• dbSNP Id: rs1652073172
• gnomAD v3: 1-152307670-CT-C
• gnomAD v4: 1-152307670-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307671del , CM000663.2:g.152307671del	GRCh38
NC_000001.10:g.152280147del , CM000663.1:g.152280147del	GRCh37
NC_000001.9:g.150546771del	NCBI36
NG_016190.1:g.22533del , LRG_1028:g.22533del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.7215del MANE Select	ENSP00000357789.1:p.Gly2406GlufsTer13
ENST00000368799.1:c.7215del	ENSP00000357789.1:p.Gly2406GlufsTer13
NM_002016.1:c.7215del , LRG_1028t1:c.7215del	NP_002007.1:p.Gly2406GlufsTer13
XM_011509329.1:c.7215del	XP_011507631.1:p.Gly2406GlufsTer13
NM_002016.2:c.7215del MANE Select	NP_002007.1:p.Gly2406GlufsTer13