Canonical Allele Identifier: CA1142048012
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304933A= , CM000663.2:g.152304933A= GRCh38
NC_000001.10:g.152277409A= , CM000663.1:g.152277409A= GRCh37
NC_000001.9:g.150544033A= NCBI36
NG_016190.1:g.25271T= , LRG_1028:g.25271T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9953T= MANE Select ENSP00000357789.1:p.Ile3318=
ENST00000368799.1:c.9953T= ENSP00000357789.1:p.Ile3318=
NM_002016.1:c.9953T= , LRG_1028t1:c.9953T= NP_002007.1:p.Ile3318=
XM_011509329.1:c.9108+845T= XP_011507631.1:n.9108+845T=
NM_002016.2:c.9953T= MANE Select NP_002007.1:p.Ile3318=