Canonical Allele Identifier: CA1143900182
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304860A= , CM000663.2:g.152304860A= GRCh38
NC_000001.10:g.152277336A= , CM000663.1:g.152277336A= GRCh37
NC_000001.9:g.150543960A= NCBI36
NG_016190.1:g.25344T= , LRG_1028:g.25344T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10026T= MANE Select ENSP00000357789.1:p.Asp3342=
ENST00000368799.1:c.10026T= ENSP00000357789.1:p.Asp3342=
NM_002016.1:c.10026T= , LRG_1028t1:c.10026T= NP_002007.1:p.Asp3342=
XM_011509329.1:c.9108+918T= XP_011507631.1:n.9108+918T=
NM_002016.2:c.10026T= MANE Select NP_002007.1:p.Asp3342=