Canonical Allele Identifier: CA1144036201
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311444G= , CM000663.2:g.152311444G= GRCh38
NC_000001.10:g.152283920G= , CM000663.1:g.152283920G= GRCh37
NC_000001.9:g.150550544G= NCBI36
NG_016190.1:g.18760C= , LRG_1028:g.18760C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3442C= MANE Select ENSP00000357789.1:p.Gln1148=
ENST00000368799.1:c.3442C= ENSP00000357789.1:p.Gln1148=
NM_002016.1:c.3442C= , LRG_1028t1:c.3442C= NP_002007.1:p.Gln1148=
XM_011509329.1:c.3442C= XP_011507631.1:p.Gln1148=
NM_002016.2:c.3442C= MANE Select NP_002007.1:p.Gln1148=