Canonical Allele Identifier: CA2574057965
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304654_152304679del , CM000663.2:g.152304654_152304679del GRCh38
NC_000001.10:g.152277130_152277155del , CM000663.1:g.152277130_152277155del GRCh37
NC_000001.9:g.150543754_150543779del NCBI36
NG_016190.1:g.25526_25551del , LRG_1028:g.25526_25551del

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10208_10233del MANE Select ENSP00000357789.1:p.Thr3403ArgfsTer?
ENST00000368799.1:c.10208_10233del ENSP00000357789.1:p.Thr3403ArgfsTer?
NM_002016.1:c.10208_10233del , LRG_1028t1:c.10208_10233del NP_002007.1:p.Thr3403ArgfsTer?
XM_011509329.1:c.9109-845_9109-820del XP_011507631.1:n.9109-845_9109-820del
NM_002016.2:c.10208_10233del MANE Select NP_002007.1:p.Thr3403ArgfsTer?