Canonical Allele Identifier: CA2647993634
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309003_152309014del , CM000663.2:g.152309003_152309014del GRCh38
NC_000001.10:g.152281479_152281490del , CM000663.1:g.152281479_152281490del GRCh37
NC_000001.9:g.150548103_150548114del NCBI36
NG_016190.1:g.21191_21202del , LRG_1028:g.21191_21202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5873_5884del MANE Select ENSP00000357789.1:p.Gly1958_His1961del
ENST00000368799.1:c.5873_5884del ENSP00000357789.1:p.Gly1958_His1961del
NM_002016.1:c.5873_5884del , LRG_1028t1:c.5873_5884del NP_002007.1:p.Gly1958_His1961del
XM_011509329.1:c.5873_5884del XP_011507631.1:p.Gly1958_His1961del
NM_002016.2:c.5873_5884del MANE Select NP_002007.1:p.Gly1958_His1961del