Canonical Allele Identifier: CA2479947714
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304907C= , CM000663.2:g.152304907C= GRCh38
NC_000001.10:g.152277383C= , CM000663.1:g.152277383C= GRCh37
NC_000001.9:g.150544007C= NCBI36
NG_016190.1:g.25297G= , LRG_1028:g.25297G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9979G= MANE Select ENSP00000357789.1:p.Val3327=
ENST00000368799.1:c.9979G= ENSP00000357789.1:p.Val3327=
NM_002016.1:c.9979G= , LRG_1028t1:c.9979G= NP_002007.1:p.Val3327=
XM_011509329.1:c.9108+871G= XP_011507631.1:n.9108+871G=
NM_002016.2:c.9979G= MANE Select NP_002007.1:p.Val3327=