Canonical Allele Identifier: CA2479950135

Gene: FLG

Linked Data

• dbSNP Id: rs1652209355

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152309186_152309190del , CM000663.2:g.152309186_152309190del	GRCh38
NC_000001.10:g.152281662_152281666del , CM000663.1:g.152281662_152281666del	GRCh37
NC_000001.9:g.150548286_150548290del	NCBI36
NG_016190.1:g.21014_21018del , LRG_1028:g.21014_21018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.5696_5700del MANE Select	ENSP00000357789.1:p.Gln1899ArgfsTer19
ENST00000368799.1:c.5696_5700del	ENSP00000357789.1:p.Gln1899ArgfsTer19
NM_002016.1:c.5696_5700del , LRG_1028t1:c.5696_5700del	NP_002007.1:p.Gln1899ArgfsTer19
XM_011509329.1:c.5696_5700del	XP_011507631.1:p.Gln1899ArgfsTer19
NM_002016.2:c.5696_5700del MANE Select	NP_002007.1:p.Gln1899ArgfsTer19