Canonical Allele Identifier: CA2479947482
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304514C= , CM000663.2:g.152304514C= GRCh38
NC_000001.10:g.152276990C= , CM000663.1:g.152276990C= GRCh37
NC_000001.9:g.150543614C= NCBI36
NG_016190.1:g.25690G= , LRG_1028:g.25690G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10372G= MANE Select ENSP00000357789.1:p.Gly3458=
ENST00000368799.1:c.10372G= ENSP00000357789.1:p.Gly3458=
NM_002016.1:c.10372G= , LRG_1028t1:c.10372G= NP_002007.1:p.Gly3458=
XM_011509329.1:c.9109-681G= XP_011507631.1:n.9109-681G=
NM_002016.2:c.10372G= MANE Select NP_002007.1:p.Gly3458=