Canonical Allele Identifier: CA1147518763
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311416G= , CM000663.2:g.152311416G= GRCh38
NC_000001.10:g.152283892G= , CM000663.1:g.152283892G= GRCh37
NC_000001.9:g.150550516G= NCBI36
NG_016190.1:g.18788C= , LRG_1028:g.18788C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3470C= MANE Select ENSP00000357789.1:p.Ala1157=
ENST00000368799.1:c.3470C= ENSP00000357789.1:p.Ala1157=
NM_002016.1:c.3470C= , LRG_1028t1:c.3470C= NP_002007.1:p.Ala1157=
XM_011509329.1:c.3470C= XP_011507631.1:p.Ala1157=
NM_002016.2:c.3470C= MANE Select NP_002007.1:p.Ala1157=