Canonical Allele Identifier: CA30558194

Gene: FLG

Linked Data

• dbSNP Id: rs35725667

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311553dup , CM000663.2:g.152311553dup	GRCh38
NC_000001.10:g.152284029dup , CM000663.1:g.152284029dup	GRCh37
NC_000001.9:g.150550653dup	NCBI36
NG_016190.1:g.18651dup , LRG_1028:g.18651dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3333dup MANE Select	ENSP00000357789.1:p.Gly1112TrpfsTer14
ENST00000368799.1:c.3333dup	ENSP00000357789.1:p.Gly1112TrpfsTer14
NM_002016.1:c.3333dup , LRG_1028t1:c.3333dup	NP_002007.1:p.Gly1112TrpfsTer14
XM_011509329.1:c.3333dup	XP_011507631.1:p.Gly1112TrpfsTer14
NM_002016.2:c.3333dup MANE Select	NP_002007.1:p.Gly1112TrpfsTer14