Canonical Allele Identifier: CA2647993512
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304673_152304689del , CM000663.2:g.152304673_152304689del GRCh38
NC_000001.10:g.152277149_152277165del , CM000663.1:g.152277149_152277165del GRCh37
NC_000001.9:g.150543773_150543789del NCBI36
NG_016190.1:g.25518_25534del , LRG_1028:g.25518_25534del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10200_10216del MANE Select ENSP00000357789.1:p.His3400GlnfsTer?
ENST00000368799.1:c.10200_10216del ENSP00000357789.1:p.His3400GlnfsTer?
NM_002016.1:c.10200_10216del , LRG_1028t1:c.10200_10216del NP_002007.1:p.His3400GlnfsTer?
XM_011509329.1:c.9109-853_9109-837del XP_011507631.1:n.9109-853_9109-837del
NM_002016.2:c.10200_10216del MANE Select NP_002007.1:p.His3400GlnfsTer?