Canonical Allele Identifier: CA1103270
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs758310303
ExAC: 1:152276774 TG / T
gnomAD v2: 1-152276774-TG-T
gnomAD v3: 1-152304298-TG-T
gnomAD v4: 1-152304298-TG-T
MyVariant Identifiers: chr1:g.152276775del (hg19) chr1:g.152304299del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304301del , CM000663.2:g.152304301del GRCh38
NC_000001.10:g.152276777del , CM000663.1:g.152276777del GRCh37
NC_000001.9:g.150543401del NCBI36
NG_016190.1:g.25905del , LRG_1028:g.25905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10587del MANE Select ENSP00000357789.1:p.Arg3530GlyfsTer?
ENST00000368799.1:c.10587del ENSP00000357789.1:p.Arg3530GlyfsTer?
NM_002016.1:c.10587del , LRG_1028t1:c.10587del NP_002007.1:p.Arg3530GlyfsTer?
XM_011509329.1:c.9109-466del XP_011507631.1:n.9109-466del
NM_002016.2:c.10587del MANE Select NP_002007.1:p.Arg3530GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'