Canonical Allele Identifier: CA2479947567
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1651824568

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304672dup , CM000663.2:g.152304672dup GRCh38
NC_000001.10:g.152277148dup , CM000663.1:g.152277148dup GRCh37
NC_000001.9:g.150543772dup NCBI36
NG_016190.1:g.25533dup , LRG_1028:g.25533dup

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10215dup MANE Select ENSP00000357789.1:p.Ser3406GlnfsTer?
ENST00000368799.1:c.10215dup ENSP00000357789.1:p.Ser3406GlnfsTer?
NM_002016.1:c.10215dup , LRG_1028t1:c.10215dup NP_002007.1:p.Ser3406GlnfsTer?
XM_011509329.1:c.9109-838dup XP_011507631.1:n.9109-838dup
NM_002016.2:c.10215dup MANE Select NP_002007.1:p.Ser3406GlnfsTer?