Canonical Allele Identifier: CA2647993477

Gene: FLG

Linked Data

• gnomAD v4: 1-152307660-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152307660_152307661insT , CM000663.2:g.152307660_152307661insT	GRCh38
NC_000001.10:g.152280136_152280137insT , CM000663.1:g.152280136_152280137insT	GRCh37
NC_000001.9:g.150546760_150546761insT	NCBI36
NG_016190.1:g.22543_22544insA , LRG_1028:g.22543_22544insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.7225_7226insA MANE Select	ENSP00000357789.1:p.Gly2409GlufsTer14
ENST00000368799.1:c.7225_7226insA	ENSP00000357789.1:p.Gly2409GlufsTer14
NM_002016.1:c.7225_7226insA , LRG_1028t1:c.7225_7226insA	NP_002007.1:p.Gly2409GlufsTer14
XM_011509329.1:c.7225_7226insA	XP_011507631.1:p.Gly2409GlufsTer14
NM_002016.2:c.7225_7226insA MANE Select	NP_002007.1:p.Gly2409GlufsTer14