Canonical Allele Identifier: CA1007766878
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652496803

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312244del , CM000663.2:g.152312244del GRCh38
NC_000001.10:g.152284720del , CM000663.1:g.152284720del GRCh37
NC_000001.9:g.150551344del NCBI36
NG_016190.1:g.17960del , LRG_1028:g.17960del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2642del MANE Select ENSP00000357789.1:p.Asp881ValfsTer?
ENST00000368799.1:c.2642del ENSP00000357789.1:p.Asp881ValfsTer?
NM_002016.1:c.2642del , LRG_1028t1:c.2642del NP_002007.1:p.Asp881ValfsTer?
XM_011509329.1:c.2642del XP_011507631.1:p.Asp881ValfsTer?
NM_002016.2:c.2642del MANE Select NP_002007.1:p.Asp881ValfsTer?