Canonical Allele Identifier: CA2647993748
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312270_152312273dup , CM000663.2:g.152312270_152312273dup GRCh38
NC_000001.10:g.152284746_152284749dup , CM000663.1:g.152284746_152284749dup GRCh37
NC_000001.9:g.150551370_150551373dup NCBI36
NG_016190.1:g.17933_17936dup , LRG_1028:g.17933_17936dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2615_2618dup MANE Select ENSP00000357789.1:p.His873GlnfsTer10
ENST00000368799.1:c.2615_2618dup ENSP00000357789.1:p.His873GlnfsTer10
NM_002016.1:c.2615_2618dup , LRG_1028t1:c.2615_2618dup NP_002007.1:p.His873GlnfsTer10
XM_011509329.1:c.2615_2618dup XP_011507631.1:p.His873GlnfsTer10
NM_002016.2:c.2615_2618dup MANE Select NP_002007.1:p.His873GlnfsTer10