Canonical Allele Identifier: CA1007765981

Gene: FLG

Linked Data

• dbSNP Id: rs1652355324
• gnomAD v3: 1-152310798-T-TGGA
• gnomAD v4: 1-152310798-T-TGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310799_152310800insGAG , CM000663.2:g.152310799_152310800insGAG	GRCh38
NC_000001.10:g.152283275_152283276insGAG , CM000663.1:g.152283275_152283276insGAG	GRCh37
NC_000001.9:g.150549899_150549900insGAG	NCBI36
NG_016190.1:g.19405_19406insTCC , LRG_1028:g.19405_19406insTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.4087_4088insTCC MANE Select	ENSP00000357789.1:p.Gln1362_Gln1363insLeu
ENST00000368799.1:c.4087_4088insTCC	ENSP00000357789.1:p.Gln1362_Gln1363insLeu
NM_002016.1:c.4087_4088insTCC , LRG_1028t1:c.4087_4088insTCC	NP_002007.1:p.Gln1362_Gln1363insLeu
XM_011509329.1:c.4087_4088insTCC	XP_011507631.1:p.Gln1362_Gln1363insLeu
NM_002016.2:c.4087_4088insTCC MANE Select	NP_002007.1:p.Gln1362_Gln1363insLeu