Canonical Allele Identifier: CA2647993650
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311383dup , CM000663.2:g.152311383dup GRCh38
NC_000001.10:g.152283859dup , CM000663.1:g.152283859dup GRCh37
NC_000001.9:g.150550483dup NCBI36
NG_016190.1:g.18821dup , LRG_1028:g.18821dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3503dup MANE Select ENSP00000357789.1:p.His1168GlnfsTer15
ENST00000368799.1:c.3503dup ENSP00000357789.1:p.His1168GlnfsTer15
NM_002016.1:c.3503dup , LRG_1028t1:c.3503dup NP_002007.1:p.His1168GlnfsTer15
XM_011509329.1:c.3503dup XP_011507631.1:p.His1168GlnfsTer15
NM_002016.2:c.3503dup MANE Select NP_002007.1:p.His1168GlnfsTer15