Canonical Allele Identifier: CA1145004642
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310473C= , CM000663.2:g.152310473C= GRCh38
NC_000001.10:g.152282949C= , CM000663.1:g.152282949C= GRCh37
NC_000001.9:g.150549573C= NCBI36
NG_016190.1:g.19731G= , LRG_1028:g.19731G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4413G= MANE Select ENSP00000357789.1:p.Glu1471=
ENST00000368799.1:c.4413G= ENSP00000357789.1:p.Glu1471=
NM_002016.1:c.4413G= , LRG_1028t1:c.4413G= NP_002007.1:p.Glu1471=
XM_011509329.1:c.4413G= XP_011507631.1:p.Glu1471=
NM_002016.2:c.4413G= MANE Select NP_002007.1:p.Glu1471=