Canonical Allele Identifier: CA2479947713
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304906A= , CM000663.2:g.152304906A= GRCh38
NC_000001.10:g.152277382A= , CM000663.1:g.152277382A= GRCh37
NC_000001.9:g.150544006A= NCBI36
NG_016190.1:g.25298T= , LRG_1028:g.25298T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9980T= MANE Select ENSP00000357789.1:p.Val3327=
ENST00000368799.1:c.9980T= ENSP00000357789.1:p.Val3327=
NM_002016.1:c.9980T= , LRG_1028t1:c.9980T= NP_002007.1:p.Val3327=
XM_011509329.1:c.9108+872T= XP_011507631.1:n.9108+872T=
NM_002016.2:c.9980T= MANE Select NP_002007.1:p.Val3327=