Canonical Allele Identifier: CA2647993540
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304762_152304858del , CM000663.2:g.152304762_152304858del GRCh38
NC_000001.10:g.152277238_152277334del , CM000663.1:g.152277238_152277334del GRCh37
NC_000001.9:g.150543862_150543958del NCBI36
NG_016190.1:g.25348_25444del , LRG_1028:g.25348_25444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10030_10126del MANE Select ENSP00000357789.1:p.Glu3344GlnfsTer15
ENST00000368799.1:c.10030_10126del ENSP00000357789.1:p.Glu3344GlnfsTer15
NM_002016.1:c.10030_10126del , LRG_1028t1:c.10030_10126del NP_002007.1:p.Glu3344GlnfsTer15
XM_011509329.1:c.9108+922_9109-927del XP_011507631.1:n.9108+922_9109-927del
NM_002016.2:c.10030_10126del MANE Select NP_002007.1:p.Glu3344GlnfsTer15