Canonical Allele Identifier: CA2479949256
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652072178
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307661dup , CM000663.2:g.152307661dup GRCh38
NC_000001.10:g.152280137dup , CM000663.1:g.152280137dup GRCh37
NC_000001.9:g.150546761dup NCBI36
NG_016190.1:g.22544dup , LRG_1028:g.22544dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7226dup MANE Select ENSP00000357789.1:p.Arg2410ThrfsTer13
ENST00000368799.1:c.7226dup ENSP00000357789.1:p.Arg2410ThrfsTer13
NM_002016.1:c.7226dup , LRG_1028t1:c.7226dup NP_002007.1:p.Arg2410ThrfsTer13
XM_011509329.1:c.7226dup XP_011507631.1:p.Arg2410ThrfsTer13
NM_002016.2:c.7226dup MANE Select NP_002007.1:p.Arg2410ThrfsTer13
Search 100 bp 5'
Search 100 bp 3'