Canonical Allele Identifier: CA2604727343
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304545_152304568del , CM000663.2:g.152304545_152304568del GRCh38
NC_000001.10:g.152277021_152277044del , CM000663.1:g.152277021_152277044del GRCh37
NC_000001.9:g.150543645_150543668del NCBI36
NG_016190.1:g.25638_25661del , LRG_1028:g.25638_25661del

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10320_10343del MANE Select ENSP00000357789.1:p.Ser3441_Ser3448del
ENST00000368799.1:c.10320_10343del ENSP00000357789.1:p.Ser3441_Ser3448del
NM_002016.1:c.10320_10343del , LRG_1028t1:c.10320_10343del NP_002007.1:p.Ser3441_Ser3448del
XM_011509329.1:c.9109-733_9109-710del XP_011507631.1:n.9109-733_9109-710del
NM_002016.2:c.10320_10343del MANE Select NP_002007.1:p.Ser3441_Ser3448del